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dbVar

Database of genomic structural variation

nsv5972396

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: 285 SVs from 28 studies. See in: genome view

Submitted genomic18,674,579-18,674,579

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5972396	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	18,674,579	18,674,579
nsv5972396	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	20,046,897	20,046,897

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17390591	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17390591	Submitted genomic		NC_000021.9:g.1867 4579_18674580ins13 1	GRCh38 (hg38)		NC_000021.9	Chr21	18,674,579	18,674,579
nssv17390591	Remapped	Perfect	NC_000021.8:g.2004 6897_20046898ins13 1	GRCh37.p13	First Pass	NC_000021.8	Chr21	20,046,897	20,046,897

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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