A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611887



Internal ID21803934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73491150..73491467hg38UCSC Ensembl
chr15:73783491..73783808hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031394
Supporting Variants
Samples
Known GenesC15orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611887
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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