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dbVar

Database of genomic structural variation

nsv5659346

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: 150 SVs from 28 studies. See in: genome view

Submitted genomic57,002,874-57,002,874

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659346	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	57,002,874	57,002,874
nsv5659346	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	55,080,235	55,080,235

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17090811	insertion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17090811	Submitted genomic		NC_000017.11:g.570 02874_57002875ins1 522	GRCh38 (hg38)		NC_000017.11	Chr17	57,002,874	57,002,874
nssv17090811	Remapped	Perfect	NC_000017.10:g.550 80235_55080236ins1 522	GRCh37.p13	First Pass	NC_000017.10	Chr17	55,080,235	55,080,235

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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