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dbVar

Database of genomic structural variation

nsv5959371

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: 107 SVs from 24 studies. See in: genome view

Submitted genomic77,041,788-77,041,788

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5959371	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	77,041,788	77,041,788
nsv5959371	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	76,337,613	76,337,613

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17418045	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17418045	Submitted genomic		NC_000005.10:g.770 41788_77041789ins1 32	GRCh38 (hg38)		NC_000005.10	Chr5	77,041,788	77,041,788
nssv17418045	Remapped	Perfect	NC_000005.9:g.7633 7613_76337614ins13 2	GRCh37.p13	First Pass	NC_000005.9	Chr5	76,337,613	76,337,613

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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