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dbVar

Database of genomic structural variation

nsv1159920

Organism: Homo sapiens

Study:nstd111 (Lou et al. 2015)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:189,484

Publication(s):Lou et al. 2015

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: 474 SVs from 68 studies. See in: genome view

Remapped(Score: Perfect):91,907,262-92,096,745

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv1159920	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	91,907,262	91,913,416	92,093,243	92,096,745
nsv1159920	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	91,640,428	91,646,582	91,826,409	91,829,911

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv4030810	deletion	SNP array	Probe signal intensity	1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv4030810	Remapped	Perfect	NC_000011.10:g.(91 907262_91913416)_( 92093243_92096745) del	GRCh38.p12	First Pass	NC_000011.10	Chr11	91,907,262	91,913,416	92,093,243	92,096,745
nssv4030810	Submitted genomic		NC_000011.9:g.(916 40428_91646582)_(9 1826409_91829911)d el	GRCh37 (hg19)		NC_000011.9	Chr11	91,640,428	91,646,582	91,826,409	91,829,911

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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