A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17713617



Internal ID137283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:51663231..51663270hg38UCSC Ensembl
chr17:49740591..49740630hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536798
Supporting Variants
Samples
Known GenesCA10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17713617
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.71995


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