A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065951



Internal ID18808482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83160637..83175681hg38UCSC Ensembl
Innerchr16:83194242..83209286hg19UCSC Ensembl
Innerchr16:81751743..81766787hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3815045
hg1915045
hg1815045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3053n100
Supporting Variantsnssv3559875, nssv3559871, nssv3559869, nssv3559868, nssv3559866, nssv3559874, nssv3559873, nssv3559867, nssv3559870, nssv3559872
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065951
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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