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dbVar

Database of genomic structural variation

nsv5950167

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

Submitted genomic77,883,724-77,883,724

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5950167	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	77,883,724	77,883,724
nsv5950167	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	78,593,441	78,593,441

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17432788	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17432788	Submitted genomic		NC_000006.12:g.778 83724_77883725ins6 0	GRCh38 (hg38)		NC_000006.12	Chr6	77,883,724	77,883,724
nssv17432788	Remapped	Perfect	NC_000006.11:g.785 93441_78593442ins6 0	GRCh37.p13	First Pass	NC_000006.11	Chr6	78,593,441	78,593,441

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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