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dbVar

Database of genomic structural variation

nsv5950997

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: 114 SVs from 21 studies. See in: genome view

Submitted genomic79,667,940-79,667,940

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5950997	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	79,667,940	79,667,940
nsv5950997	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	82,282,855	82,282,855

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17440767	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17440767	Submitted genomic		NC_000009.12:g.796 67940_79667941ins1 81	GRCh38 (hg38)		NC_000009.12	Chr9	79,667,940	79,667,940
nssv17440767	Remapped	Perfect	NC_000009.11:g.822 82855_82282856ins1 81	GRCh37.p13	First Pass	NC_000009.11	Chr9	82,282,855	82,282,855

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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