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

dbVar

Database of genomic structural variation

nsv3071706

Organism: Homo sapiens

Study:nstd90 (dbSNP curated variants)
Variant Type:insertion
Method Type:Curated
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:3

Data Source:HUMANGENOME_JCVI

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: 387 SVs from 45 studies. See in: genome view

Remapped(Score: Perfect):1,642,369-1,642,369

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3071706	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	1,642,369	1,642,369
nsv3071706	Remapped	Pass	GRCh38.p12	ALT_REF_LOCI_3	Second Pass	NT_187680.1	Chr8\|NT_18 7680.1	55,309	55,311
nsv3071706	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	1,590,535	1,590,535

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis
nssv14042733	insertion	1104685105690	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14042733	Remapped	Pass	NT_187680.1:g.5530 9_55311ins217	GRCh38.p12	Second Pass	NT_187680.1	Chr8\|NT_18 7680.1	55,309	55,311
nssv14042733	Remapped	Perfect	NC_000008.11:g.164 2369_1642370ins217	GRCh38.p12	First Pass	NC_000008.11	Chr8	1,642,369	1,642,369
nssv14042733	Submitted genomic		NC_000008.10:g.159 0535_1590536ins217	GRCh37 (hg19)		NC_000008.10	Chr8	1,590,535	1,590,535

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

You are here: NCBI