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dbVar

Database of genomic structural variation

nsv5664190

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: 136 SVs from 25 studies. See in: genome view

Submitted genomic38,540,486-38,540,486

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5664190	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	38,540,486	38,540,486
nsv5664190	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	39,031,126	39,031,126

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17104660	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
nssv17104660	Submitted genomic		NC_000019.10:g.385 40486_38540487ins1 46	GRCh38 (hg38)		NC_000019.10	Chr19	38,540,486	38,540,486
nssv17104660	Remapped	Perfect	NC_000019.9:g.3903 1126_39031127ins14 6	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,031,126	39,031,126

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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