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dbVar

Database of genomic structural variation

nsv5974719

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: 91 SVs from 23 studies. See in: genome view

Submitted genomic89,929,046-89,929,046

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5974719	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	89,929,046	89,929,046
nsv5974719	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	90,395,390	90,395,390

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17372741	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17372741	Submitted genomic		NC_000014.9:g.8992 9046_89929047ins50	GRCh38 (hg38)		NC_000014.9	Chr14	89,929,046	89,929,046
nssv17372741	Remapped	Perfect	NC_000014.8:g.9039 5390_90395391ins50	GRCh37.p13	First Pass	NC_000014.8	Chr14	90,395,390	90,395,390

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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