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dbVar

Database of genomic structural variation

nsv5653837

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

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

Submitted genomic56,444,834-56,444,834

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653837	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	56,444,834	56,444,834
nsv5653837	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	56,956,203	56,956,203

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17106414	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17106414	Submitted genomic		NC_000019.10:g.564 44834_56444835ins7 48	GRCh38 (hg38)		NC_000019.10	Chr19	56,444,834	56,444,834
nssv17106414	Remapped	Perfect	NC_000019.9:g.5695 6203_56956204ins74 8	GRCh37.p13	First Pass	NC_000019.9	Chr19	56,956,203	56,956,203

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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