A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573391



Internal ID16014114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83162838..83174417hg38UCSC Ensembl
Innerchr16:83196443..83208022hg19UCSC Ensembl
Innerchr16:81753944..81765523hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3811580
hg1911580
hg1811580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5256n54
Supporting Variantsnssv861972, nssv861975, nssv861977, nssv861971, nssv861978, nssv861974, nssv861976, nssv861969, nssv861970, nssv861973
Samples
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573391
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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