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dbVar

Database of genomic structural variation

nsv4659532

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:21,700

Description:nsv4580248 from DECIPHER Consensus CNVs. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 1337 SVs from 99 studies. See in: genome view

Remapped(Score: Perfect):196,803,471-196,825,170

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4659532	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	196,803,471	196,825,170
nsv4659532	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	196,772,601	196,794,300

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16203819	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16203819	Remapped	Perfect	NC_000001.11:g.(?_ 196803471)_(196825 170_?)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	196,803,471	196,825,170
nssv16203819	Submitted genomic		NC_000001.10:g.(?_ 196772601)_(196794 300_?)del	GRCh37 (hg19)		NC_000001.10	Chr1	196,772,601	196,794,300

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16203819	0.21	397	1892

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