A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060089



Internal ID18802620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83162620..83177339hg38UCSC Ensembl
Innerchr16:83196225..83210944hg19UCSC Ensembl
Innerchr16:81753726..81768445hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3814720
hg1914720
hg1814720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3053n100
Supporting Variantsnssv3559927, nssv3559929, nssv3559928
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)nsv1060089
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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