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dbVar

Database of genomic structural variation

nsv5610547

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: 134 SVs from 26 studies. See in: genome view

Submitted genomic215,134,251-215,134,251

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5610547	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	215,134,251	215,134,251
nsv5610547	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	215,998,974	215,998,974

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17111248	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17111248	Submitted genomic		NC_000002.12:g.215 134251_215134252in s73	GRCh38 (hg38)		NC_000002.12	Chr2	215,134,251	215,134,251
nssv17111248	Remapped	Perfect	NC_000002.11:g.215 998974_215998975in s73	GRCh37.p13	First Pass	NC_000002.11	Chr2	215,998,974	215,998,974

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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