Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4660769

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:4,707

Description:nsv4608186 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: 145 SVs from 40 studies. See in: genome view

Remapped(Score: Perfect):100,600,978-100,605,684

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4660769	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	100,600,978	100,605,684
nsv4660769	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	100,198,601	100,203,307

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16200787	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16200787	Remapped	Perfect	NC_000007.14:g.(?_ 100600978)_(100605 684_?)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,600,978	100,605,684
nssv16200787	Submitted genomic		NC_000007.13:g.(?_ 100198601)_(100203 307_?)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,198,601	100,203,307

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)
nssv16200787	0.057	107	1892

You are here: NCBI