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dbVar

Database of genomic structural variation

nsv5665693

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: 99 SVs from 19 studies. See in: genome view

Submitted genomic10,224,772-10,224,772

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5665693	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	10,224,772	10,224,772
nsv5665693	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	10,205,420	10,205,420

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17115153	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
nssv17115153	Submitted genomic		NC_000020.11:g.102 24772_10224773ins9 54	GRCh38 (hg38)		NC_000020.11	Chr20	10,224,772	10,224,772
nssv17115153	Remapped	Perfect	NC_000020.10:g.102 05420_10205421ins9 54	GRCh37.p13	First Pass	NC_000020.10	Chr20	10,205,420	10,205,420

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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