A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564281



Internal ID16351690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35136670..35145113hg38UCSC Ensembl
Innerchr14:35605876..35614319hg19UCSC Ensembl
Innerchr14:34675627..34684070hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg388444
hg198444
hg188444
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3625n54
Supporting Variantsnssv825588, nssv825596, nssv825586, nssv825601, nssv825598, nssv825578, nssv825594, nssv825591, nssv825595, nssv825587, nssv825582, nssv825590, nssv825593, nssv825589, nssv825592, nssv825581, nssv825579, nssv825577, nssv825599, nssv825603, nssv825600, nssv825597, nssv825580, nssv825602, nssv825585, nssv825584, nssv825583
Samples
Known GenesKIAA0391
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564281
Frequency
Sample Size17421
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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