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

dbVar

Database of genomic structural variation

nsv3071833

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:1

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: 113 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):95,196,488-95,196,488

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3071833	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	95,196,488	95,196,488
nsv3071833	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	95,862,236	95,862,236

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis
nssv14038980	insertion	1104685022501	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14038980	Remapped	Perfect	NC_000002.12:g.951 96488_95196489ins9 71	GRCh38.p12	First Pass	NC_000002.12	Chr2	95,196,488	95,196,488
nssv14038980	Submitted genomic		NC_000002.11:g.958 62236_95862237ins9 71	GRCh37 (hg19)		NC_000002.11	Chr2	95,862,236	95,862,236

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