A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056016



Internal ID18798547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77990656..78129245hg38UCSC Ensembl
Innerchr16:78024553..78163142hg19UCSC Ensembl
Innerchr16:76582054..76720643hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38138590
hg19138590
hg18138590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559678, nssv3559677
Samples
Known GenesCLEC3A, WWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056016
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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