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dbVar

Database of genomic structural variation

nsv5609146

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: 93 SVs from 22 studies. See in: genome view

Submitted genomic85,294,331-85,294,331

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5609146	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	85,294,331	85,294,331
nsv5609146	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	85,521,454	85,521,454

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17115612	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
nssv17115612	Submitted genomic		NC_000002.12:g.852 94331_85294332ins3 43	GRCh38 (hg38)		NC_000002.12	Chr2	85,294,331	85,294,331
nssv17115612	Remapped	Perfect	NC_000002.11:g.855 21454_85521455ins3 43	GRCh37.p13	First Pass	NC_000002.11	Chr2	85,521,454	85,521,454

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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