A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17734610



Internal ID158276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30841808..30930000hg38UCSC Ensembl
chr21:32214127..32302319hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3888193
hg1988193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539202
Supporting Variants
Samples
Known GenesKRTAP11-1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17734610
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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