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dbVar

Database of genomic structural variation

nsv5621229

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: 176 SVs from 28 studies. See in: genome view

Submitted genomic11,967,616-11,967,616

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5621229	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	11,967,616	11,967,616
nsv5621229	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	12,027,673	12,027,673

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17060172	insertion	HG03732	Sequencing	Sequence alignment	1,582

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17060172	Submitted genomic		NC_000001.11:g.119 67616_11967617ins8 1	GRCh38 (hg38)		NC_000001.11	Chr1	11,967,616	11,967,616
nssv17060172	Remapped	Perfect	NC_000001.10:g.120 27673_12027674ins8 1	GRCh37.p13	First Pass	NC_000001.10	Chr1	12,027,673	12,027,673

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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