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dbVar

Database of genomic structural variation

nsv5964132

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: 86 SVs from 21 studies. See in: genome view

Submitted genomic156,471,927-156,471,927

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5964132	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	156,471,927	156,471,927
nsv5964132	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	155,898,937	155,898,937

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17428503	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17428503	Submitted genomic		NC_000005.10:g.156 471927_156471928in s329	GRCh38 (hg38)		NC_000005.10	Chr5	156,471,927	156,471,927
nssv17428503	Remapped	Perfect	NC_000005.9:g.1558 98937_155898938ins 329	GRCh37.p13	First Pass	NC_000005.9	Chr5	155,898,937	155,898,937

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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