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dbVar

Database of genomic structural variation

nsv5671951

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: 117 SVs from 27 studies. See in: genome view

Submitted genomic37,656,829-37,656,829

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5671951	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	37,656,829	37,656,829
nsv5671951	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	38,052,836	38,052,836

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17121120	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17121120	Submitted genomic		NC_000022.11:g.376 56829_37656830ins3 09	GRCh38 (hg38)		NC_000022.11	Chr22	37,656,829	37,656,829
nssv17121120	Remapped	Perfect	NC_000022.10:g.380 52836_38052837ins3 09	GRCh37.p13	First Pass	NC_000022.10	Chr22	38,052,836	38,052,836

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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