A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684116



Internal ID15420768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:81328185..81334384hg38UCSC Ensembl
Innerchr15:81620526..81626725hg19UCSC Ensembl
Innerchr15:79407581..79413780hg18UCSC Ensembl
Innerchr15:79407581..79413780hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg386200
hg196200
hg186200
hg176200
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520339
Supporting Variants
Samples
Known GenesTMC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684116
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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