A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701036



Internal ID124702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73713030..73713091hg38UCSC Ensembl
chr15:74005371..74005432hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533708
Supporting Variants
Samples
Known GenesCD276
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701036
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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