A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704416



Internal ID128082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79924533..79953030hg38UCSC Ensembl
chr15:80216875..80245372hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3828498
hg1928498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5522730
Supporting Variants
Samples
Known GenesC15orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704416
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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