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dbVar

Database of genomic structural variation

nsv5657685

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: 148 SVs from 29 studies. See in: genome view

Submitted genomic69,298,233-69,298,233

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657685	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	69,298,233	69,298,233
nsv5657685	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	67,294,374	67,294,374

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17089537	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
nssv17089537	Submitted genomic		NC_000017.11:g.692 98233_69298234ins9 6	GRCh38 (hg38)		NC_000017.11	Chr17	69,298,233	69,298,233
nssv17089537	Remapped	Perfect	NC_000017.10:g.672 94374_67294375ins9 6	GRCh37.p13	First Pass	NC_000017.10	Chr17	67,294,374	67,294,374

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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