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dbVar

Database of genomic structural variation

nsv5669343

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: 446 SVs from 58 studies. See in: genome view

Submitted genomic42,511,750-42,511,750

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5669343	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	42,511,750	42,511,750
nsv5669343	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	42,907,756	42,907,756

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17125956	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17125956	Submitted genomic		NC_000022.11:g.425 11750_42511751ins2 74	GRCh38 (hg38)		NC_000022.11	Chr22	42,511,750	42,511,750
nssv17125956	Remapped	Perfect	NC_000022.10:g.429 07756_42907757ins2 74	GRCh37.p13	First Pass	NC_000022.10	Chr22	42,907,756	42,907,756

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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