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dbVar

Database of genomic structural variation

nsv5668933

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: 219 SVs from 23 studies. See in: genome view

Submitted genomic45,208,500-45,208,500

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5668933	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	45,208,500	45,208,500
nsv5668933	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	45,604,381	45,604,381

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17131687	insertion	SAMN00004622	Sequencing	Sequence alignment	1,208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17131687	Submitted genomic		NC_000022.11:g.452 08500_45208501ins1 62	GRCh38 (hg38)		NC_000022.11	Chr22	45,208,500	45,208,500
nssv17131687	Remapped	Perfect	NC_000022.10:g.456 04381_45604382ins1 62	GRCh37.p13	First Pass	NC_000022.10	Chr22	45,604,381	45,604,381

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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