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dbVar

Database of genomic structural variation

nsv5652423

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: 100 SVs from 30 studies. See in: genome view

Submitted genomic47,718,899-47,718,899

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5652423	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	47,718,899	47,718,899
nsv5652423	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	48,222,156	48,222,156

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17105466	insertion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17105466	Submitted genomic		NC_000019.10:g.477 18899_47718900ins7 2	GRCh38 (hg38)		NC_000019.10	Chr19	47,718,899	47,718,899
nssv17105466	Remapped	Perfect	NC_000019.9:g.4822 2156_48222157ins72	GRCh37.p13	First Pass	NC_000019.9	Chr19	48,222,156	48,222,156

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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