A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17047633



Internal ID99630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67251614..67251864hg38UCSC Ensembl
chr11:67019085..67019335hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506904
Supporting Variants
Samples
Known GenesKDM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17047633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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