A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565948



Internal ID16353357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:102467010..102565494hg38UCSC Ensembl
Innerchr14:102933347..103031831hg19UCSC Ensembl
Innerchr14:102003100..102101584hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3898485
hg1998485
hg1898485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148705, nssv1148706
SamplesHGDP00615, HGDP00628
Known GenesANKRD9, MIR4309, TECPR2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565948
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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