A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17058784



Internal ID107052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:52604309..52618589hg38UCSC Ensembl
chr12:52998093..53012373hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3814281
hg1914281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502897
Supporting Variants
Samples
Known GenesKRT73
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17058784
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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