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dbVar

Database of genomic structural variation

nsv5978851

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: 249 SVs from 26 studies. See in: genome view

Submitted genomic29,900,461-29,900,461

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5978851	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	29,900,461	29,900,461
nsv5978851	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	31,272,778	31,272,778

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17403825	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17403825	Submitted genomic		NC_000021.9:g.2990 0461_29900462ins17 6	GRCh38 (hg38)		NC_000021.9	Chr21	29,900,461	29,900,461
nssv17403825	Remapped	Perfect	NC_000021.8:g.3127 2778_31272779ins17 6	GRCh37.p13	First Pass	NC_000021.8	Chr21	31,272,778	31,272,778

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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