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dbVar

Database of genomic structural variation

nsv5667115

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

Submitted genomic37,914,404-37,914,404

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5667115	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	37,914,404	37,914,404
nsv5667115	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	36,542,806	36,542,806

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17116223	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17116223	Submitted genomic		NC_000020.11:g.379 14404_37914405ins2 39	GRCh38 (hg38)		NC_000020.11	Chr20	37,914,404	37,914,404
nssv17116223	Remapped	Perfect	NC_000020.10:g.365 42806_36542807ins2 39	GRCh37.p13	First Pass	NC_000020.10	Chr20	36,542,806	36,542,806

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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