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dbVar

Database of genomic structural variation

nsv5974601

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: 121 SVs from 20 studies. See in: genome view

Submitted genomic119,665,093-119,665,093

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5974601	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	119,665,093	119,665,093
nsv5974601	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	121,424,605	121,424,605

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17353846	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17353846	Submitted genomic		NC_000010.11:g.119 665093_119665094in s247	GRCh38 (hg38)		NC_000010.11	Chr10	119,665,093	119,665,093
nssv17353846	Remapped	Perfect	NC_000010.10:g.121 424605_121424606in s247	GRCh37.p13	First Pass	NC_000010.10	Chr10	121,424,605	121,424,605

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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