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dbVar

Database of genomic structural variation

nsv5973174

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: 154 SVs from 30 studies. See in: genome view

Submitted genomic42,818,816-42,818,816

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5973174	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	42,818,816	42,818,816
nsv5973174	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	43,214,822	43,214,822

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17407853	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17407853	Submitted genomic		NC_000022.11:g.428 18816_42818817ins3 15	GRCh38 (hg38)		NC_000022.11	Chr22	42,818,816	42,818,816
nssv17407853	Remapped	Perfect	NC_000022.10:g.432 14822_43214823ins3 15	GRCh37.p13	First Pass	NC_000022.10	Chr22	43,214,822	43,214,822

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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