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dbVar

Database of genomic structural variation

nsv4441389

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=SIMPLEINS
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: 87 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):70,407,944-70,407,944

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4441389	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	70,407,944	70,407,944
nsv4441389	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	72,167,700	72,167,700

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15762407	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15762407	Remapped	Perfect	NC_000010.11:g.704 07944_70407945ins3 75	GRCh38.p12	First Pass	NC_000010.11	Chr10	70,407,944	70,407,944
nssv15762407	Submitted genomic		NC_000010.10:g.721 67700_72167701ins3 75	GRCh37 (hg19)		NC_000010.10	Chr10	72,167,700	72,167,700

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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