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dbVar

Database of genomic structural variation

nsv5958686

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Almarri et al. 2020

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: 205 SVs from 35 studies. See in: genome view

Submitted genomic162,947,345-162,947,345

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5958686	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	162,947,345	162,947,345
nsv5958686	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	163,368,377	163,368,377

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17414270	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17414270	Submitted genomic		NC_000006.12:g.162 947345_162947346in s91	GRCh38 (hg38)		NC_000006.12	Chr6	162,947,345	162,947,345
nssv17414270	Remapped	Perfect	NC_000006.11:g.163 368377_163368378in s91	GRCh37.p13	First Pass	NC_000006.11	Chr6	163,368,377	163,368,377

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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