A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15183426



Internal ID21322222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81323239..81323317hg38UCSC Ensembl
chr15:81615580..81615658hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3935705
Supporting Variants
SamplesHG002
Known GenesSTARD5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15183426
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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