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dbVar

Database of genomic structural variation

nsv3132841

Organism: Homo sapiens

Study:nstd151 (Exome Aggregation Consortium CNVs)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:5
Validation:Not tested
Clinical Assertions: No
Region Size:247,668

Description:
See descriptions for individual calls in download files
Publication(s):Exome Aggregation Consortium CNVs

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 528 SVs from 65 studies. See in: genome view

Remapped(Score: Perfect):33,905,611-34,153,278

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv3132841	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	33,905,611	34,153,278
nsv3132841	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	33,945,223	34,192,890

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv14151392	copy number loss	Sequencing	Read depth
nssv14154119	copy number loss	Sequencing	Read depth
nssv14155186	copy number loss	Sequencing	Read depth
nssv14164180	copy number loss	Sequencing	Read depth
nssv14169414	copy number loss	Sequencing	Read depth

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv14151392	Remapped	Perfect	NC_000007.14:g.(?_ 33905611)_(3415327 8_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	33,905,611	34,153,278
nssv14154119	Remapped	Perfect	NC_000007.14:g.(?_ 33905611)_(3415327 8_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	33,905,611	34,153,278
nssv14155186	Remapped	Perfect	NC_000007.14:g.(?_ 33905611)_(3415327 8_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	33,905,611	34,153,278
nssv14164180	Remapped	Perfect	NC_000007.14:g.(?_ 33905611)_(3415327 8_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	33,905,611	34,153,278
nssv14169414	Remapped	Perfect	NC_000007.14:g.(?_ 33905611)_(3415327 8_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	33,905,611	34,153,278
nssv14151392	Submitted genomic		NC_000007.13:g.(?_ 33945223)_(3419289 0_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	33,945,223	34,192,890
nssv14154119	Submitted genomic		NC_000007.13:g.(?_ 33945223)_(3419289 0_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	33,945,223	34,192,890
nssv14155186	Submitted genomic		NC_000007.13:g.(?_ 33945223)_(3419289 0_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	33,945,223	34,192,890
nssv14164180	Submitted genomic		NC_000007.13:g.(?_ 33945223)_(3419289 0_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	33,945,223	34,192,890
nssv14169414	Submitted genomic		NC_000007.13:g.(?_ 33945223)_(3419289 0_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	33,945,223	34,192,890

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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