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dbVar

Database of genomic structural variation

nsv5961295

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: 135 SVs from 27 studies. See in: genome view

Submitted genomic59,854,027-59,854,027

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961295	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	59,854,027	59,854,027
nsv5961295	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	60,319,699	60,319,699

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17388763	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17388763	Submitted genomic		NC_000001.11:g.598 54027_59854028ins1 81	GRCh38 (hg38)		NC_000001.11	Chr1	59,854,027	59,854,027
nssv17388763	Remapped	Perfect	NC_000001.10:g.603 19699_60319700ins1 81	GRCh37.p13	First Pass	NC_000001.10	Chr1	60,319,699	60,319,699

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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