A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066140



Internal ID18808671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83305840..83340358hg38UCSC Ensembl
Innerchr16:83339445..83373963hg19UCSC Ensembl
Innerchr16:81896946..81931464hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3834519
hg1934519
hg1834519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559931
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)nsv1066140
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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