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

dbVar

Database of genomic structural variation

nsv4658800

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:231,451

Description:nsv4582808 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: 816 SVs from 72 studies. See in: genome view

Remapped(Score: Perfect):205,034,047-205,265,497

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4658800	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	205,034,047	205,265,497
nsv4658800	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	205,898,770	206,130,221

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16190028	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16190028	Remapped	Perfect	NC_000002.12:g.(?_ 205034047)_(205265 497_?)del	GRCh38.p12	First Pass	NC_000002.12	Chr2	205,034,047	205,265,497
nssv16190028	Submitted genomic		NC_000002.11:g.(?_ 205898770)_(206130 221_?)del	GRCh37 (hg19)		NC_000002.11	Chr2	205,898,770	206,130,221

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)
nssv16190028	0.073	33	450

You are here: NCBI