A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565157



Internal ID16005880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73543861..73559754hg38UCSC Ensembl
Innerchr14:74010565..74026458hg19UCSC Ensembl
Innerchr14:73080318..73096211hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3815894
hg1915894
hg1815894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3773n54
Supporting Variantsnssv829398
Samples
Known GenesHEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565157
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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