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

dbVar

Database of genomic structural variation

nsv4636423

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:136

Description:nsv4100218 from gnomAD Structural Variants. 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: 150 SVs from 28 studies. See in: genome view

Remapped(Score: Perfect):186,786,760-186,786,895

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4636423	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	186,786,760	186,786,895
nsv4636423	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	186,504,549	186,504,684

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16157583	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16157583	Remapped	Perfect	NC_000003.12:g.186 786760_186786895du p	GRCh38.p12	First Pass	NC_000003.12	Chr3	186,786,760	186,786,895
nssv16157583	Submitted genomic		NC_000003.11:g.186 504549_186504684du p	GRCh37 (hg19)		NC_000003.11	Chr3	186,504,549	186,504,684

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)
nssv16157583	0.011	242	21642

You are here: NCBI