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dbVar

Database of genomic structural variation

nsv5949701

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: 661 SVs from 62 studies. See in: genome view

Submitted genomic89,805,221-89,805,221

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5949701	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	89,805,221	89,805,221
nsv5949701	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	89,844,031	89,844,031

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17407759	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17407759	Submitted genomic		NC_000002.12:g.898 05221_89805222ins7 2	GRCh38 (hg38)		NC_000002.12	Chr2	89,805,221	89,805,221
nssv17407759	Remapped	Perfect	NC_000002.11:g.898 44031_89844032ins7 2	GRCh37.p13	First Pass	NC_000002.11	Chr2	89,844,031	89,844,031

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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