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dbVar

Database of genomic structural variation

nsv5974469

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

Submitted genomic59,181,783-59,181,783

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5974469	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	59,181,783	59,181,783
nsv5974469	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	57,756,838	57,756,838

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17391582	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17391582	Submitted genomic		NC_000020.11:g.591 81783_59181784ins2 29	GRCh38 (hg38)		NC_000020.11	Chr20	59,181,783	59,181,783
nssv17391582	Remapped	Perfect	NC_000020.10:g.577 56838_57756839ins2 29	GRCh37.p13	First Pass	NC_000020.10	Chr20	57,756,838	57,756,838

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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