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dbVar

Database of genomic structural variation

nsv4449598

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

Remapped(Score: Perfect):241,036,077-241,036,077

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4449598	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	241,036,077	241,036,077
nsv4449598	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	241,975,494	241,975,494

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15759043	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15759043	Remapped	Perfect	NC_000002.12:g.241 036077_241036078in s52	GRCh38.p12	First Pass	NC_000002.12	Chr2	241,036,077	241,036,077
nssv15759043	Submitted genomic		NC_000002.11:g.241 975494_241975495in s52	GRCh37 (hg19)		NC_000002.11	Chr2	241,975,494	241,975,494

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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