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dbVar

Database of genomic structural variation

nsv5660902

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 genomic56,444,916-56,444,916

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660902	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	56,444,916	56,444,916
nsv5660902	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	56,956,285	56,956,285

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17106415	insertion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17106415	Submitted genomic		NC_000019.10:g.564 44916_56444917ins3 33	GRCh38 (hg38)		NC_000019.10	Chr19	56,444,916	56,444,916
nssv17106415	Remapped	Perfect	NC_000019.9:g.5695 6285_56956286ins33 3	GRCh37.p13	First Pass	NC_000019.9	Chr19	56,956,285	56,956,285

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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