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dbVar

Database of genomic structural variation

nsv6056295

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Wu et al. 2021

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: 120 SVs from 23 studies. See in: genome view

Submitted genomic64,997,150-64,997,150

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6056295	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	64,997,150	64,997,150
nsv6056295	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	65,224,284	65,224,284

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17534677	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17534677	Submitted genomic		NC_000002.12:g.649 97150_64997151ins1 254	GRCh38 (hg38)		NC_000002.12	Chr2	64,997,150	64,997,150
nssv17534677	Remapped	Perfect	NC_000002.11:g.652 24284_65224285ins1 254	GRCh37.p13	First Pass	NC_000002.11	Chr2	65,224,284	65,224,284

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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