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dbVar

Database of genomic structural variation

nsv5976798

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

Submitted genomic60,180,611-60,180,611

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5976798	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	60,180,611	60,180,611
nsv5976798	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	58,755,669	58,755,669

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17406483	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17406483	Submitted genomic		NC_000020.11:g.601 80611_60180612ins3 09	GRCh38 (hg38)		NC_000020.11	Chr20	60,180,611	60,180,611
nssv17406483	Remapped	Perfect	NC_000020.10:g.587 55669_58755670ins3 09	GRCh37.p13	First Pass	NC_000020.10	Chr20	58,755,669	58,755,669

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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