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dbVar

Database of genomic structural variation

nsv5966052

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: 241 SVs from 36 studies. See in: genome view

Submitted genomic1,673,959-1,673,959

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966052	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	1,673,959	1,673,959
nsv5966052	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	1,674,193	1,674,193

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17427597	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17427597	Submitted genomic		NC_000006.12:g.167 3959_1673960ins153	GRCh38 (hg38)		NC_000006.12	Chr6	1,673,959	1,673,959
nssv17427597	Remapped	Perfect	NC_000006.11:g.167 4193_1674194ins153	GRCh37.p13	First Pass	NC_000006.11	Chr6	1,674,193	1,674,193

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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