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dbVar

Database of genomic structural variation

nsv5953352

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: 89 SVs from 26 studies. See in: genome view

Submitted genomic38,691,041-38,691,041

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5953352	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	38,691,041	38,691,041
nsv5953352	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	38,658,817	38,658,817

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17433621	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17433621	Submitted genomic		NC_000006.12:g.386 91041_38691042ins3 31	GRCh38 (hg38)		NC_000006.12	Chr6	38,691,041	38,691,041
nssv17433621	Remapped	Perfect	NC_000006.11:g.386 58817_38658818ins3 31	GRCh37.p13	First Pass	NC_000006.11	Chr6	38,658,817	38,658,817

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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