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

dbVar

Database of genomic structural variation

nsv4655069

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:mobile element deletion
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:351

Description:esv3855357 from 1000 Genomes Consortium Phase 3 Integrated SV. 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: 235 SVs from 47 studies. See in: genome view

Remapped(Score: Perfect):117,968,519-117,968,869

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4655069	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	117,968,519	117,968,869
nsv4655069	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	118,980,758	118,981,108

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16185775	alu deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16185775	Remapped	Perfect	NC_000008.11:g.117 968519_117968869de l	GRCh38.p12	First Pass	NC_000008.11	Chr8	117,968,519	117,968,869
nssv16185775	Submitted genomic		NC_000008.10:g.118 980758_118981108de l	GRCh37 (hg19)		NC_000008.10	Chr8	118,980,758	118,981,108

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)
nssv16185775	0.343	1716	5008

You are here: NCBI