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dbVar

Database of genomic structural variation

nsv5664781

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: 460 SVs from 65 studies. See in: genome view

Submitted genomic23,855,202-23,855,202

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5664781	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	23,855,202	23,855,202
nsv5664781	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	24,197,389	24,197,389

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17130109	insertion	HG02492	Sequencing	Sequence alignment	982

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17130109	Submitted genomic		NC_000022.11:g.238 55202_23855203ins1 71	GRCh38 (hg38)		NC_000022.11	Chr22	23,855,202	23,855,202
nssv17130109	Remapped	Perfect	NC_000022.10:g.241 97389_24197390ins1 71	GRCh37.p13	First Pass	NC_000022.10	Chr22	24,197,389	24,197,389

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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