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dbVar

Database of genomic structural variation

nsv4445402

Organism: Homo sapiens

Study:nstd175 (Genome in a Bottle)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Description:SVTYPE=INS;REPTYPE=DUP
Publication(s):Genome in a Bottle

Links to Other Resources

Overlapping Genes

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: 97 SVs from 22 studies. See in: genome view

Remapped(Score: Perfect):70,813,492-70,813,492

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4445402	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	70,813,492	70,813,492
nsv4445402	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	71,280,209	71,280,209

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15765775	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15765775	Remapped	Perfect	NC_000014.9:g.7081 3492_70813493ins12 8	GRCh38.p12	First Pass	NC_000014.9	Chr14	70,813,492	70,813,492
nssv15765775	Submitted genomic		NC_000014.8:g.7128 0209_71280210ins12 8	GRCh37 (hg19)		NC_000014.8	Chr14	71,280,209	71,280,209

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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