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dbVar

Database of genomic structural variation

nsv5974599

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: 134 SVs from 31 studies. See in: genome view

Submitted genomic55,488,872-55,488,872

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5974599	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	55,488,872	55,488,872
nsv5974599	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	56,000,239	56,000,239

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17408748	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17408748	Submitted genomic		NC_000019.10:g.554 88872_55488873ins1 75	GRCh38 (hg38)		NC_000019.10	Chr19	55,488,872	55,488,872
nssv17408748	Remapped	Perfect	NC_000019.9:g.5600 0239_56000240ins17 5	GRCh37.p13	First Pass	NC_000019.9	Chr19	56,000,239	56,000,239

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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