A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731177



Internal ID154843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:15553557..15555568hg38UCSC Ensembl
chr20:15534202..15536213hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg382012
hg192012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533064
Supporting Variants
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731177
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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