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dbVar

Database of genomic structural variation

nsv5614641

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

Submitted genomic221,570,797-221,570,797

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5614641	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	221,570,797	221,570,797
nsv5614641	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	222,435,517	222,435,517

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17111557	insertion	HG01114	Sequencing	Sequence alignment	977

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17111557	Submitted genomic		NC_000002.12:g.221 570797_221570798in s85	GRCh38 (hg38)		NC_000002.12	Chr2	221,570,797	221,570,797
nssv17111557	Remapped	Perfect	NC_000002.11:g.222 435517_222435518in s85	GRCh37.p13	First Pass	NC_000002.11	Chr2	222,435,517	222,435,517

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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