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dbVar

Database of genomic structural variation

nsv5667751

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

Submitted genomic42,818,816-42,818,816

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5667751	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	42,818,816	42,818,816
nsv5667751	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	43,214,822	43,214,822

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17121705	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
nssv17121705	Submitted genomic		NC_000022.11:g.428 18816_42818817ins3 18	GRCh38 (hg38)		NC_000022.11	Chr22	42,818,816	42,818,816
nssv17121705	Remapped	Perfect	NC_000022.10:g.432 14822_43214823ins3 18	GRCh37.p13	First Pass	NC_000022.10	Chr22	43,214,822	43,214,822

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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