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dbVar

Database of genomic structural variation

nsv5653290

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: 208 SVs from 45 studies. See in: genome view

Submitted genomic16,127,543-16,127,543

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653290	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	16,127,543	16,127,543
nsv5653290	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	16,030,857	16,030,857

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17096690	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
nssv17096690	Submitted genomic		NC_000017.11:g.161 27543_16127544ins5 1	GRCh38 (hg38)		NC_000017.11	Chr17	16,127,543	16,127,543
nssv17096690	Remapped	Perfect	NC_000017.10:g.160 30857_16030858ins5 1	GRCh37.p13	First Pass	NC_000017.10	Chr17	16,030,857	16,030,857

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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