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dbVar

Database of genomic structural variation

nsv4449573

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: 159 SVs from 28 studies. See in: genome view

Remapped(Score: Perfect):25,591,140-25,591,140

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4449573	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	25,591,140	25,591,140
nsv4449573	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	25,744,074	25,744,074

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15766489	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15766489	Remapped	Perfect	NC_000012.12:g.255 91140_25591141ins1 006	GRCh38.p12	First Pass	NC_000012.12	Chr12	25,591,140	25,591,140
nssv15766489	Submitted genomic		NC_000012.11:g.257 44074_25744075ins1 006	GRCh37 (hg19)		NC_000012.11	Chr12	25,744,074	25,744,074

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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