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dbVar

Database of genomic structural variation

nsv5662770

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: 202 SVs from 20 studies. See in: genome view

Submitted genomic47,882,041-47,882,041

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5662770	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	47,882,041	47,882,041
nsv5662770	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	45,408,412	45,408,412

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17101236	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
nssv17101236	Submitted genomic		NC_000018.10:g.478 82041_47882042ins5 2	GRCh38 (hg38)		NC_000018.10	Chr18	47,882,041	47,882,041
nssv17101236	Remapped	Perfect	NC_000018.9:g.4540 8412_45408413ins52	GRCh37.p13	First Pass	NC_000018.9	Chr18	45,408,412	45,408,412

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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