A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565108



Internal ID16352517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73526665..73533785hg38UCSC Ensembl
Innerchr14:73993369..74000489hg19UCSC Ensembl
Innerchr14:73063122..73070242hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg387121
hg197121
hg187121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3760n54
Supporting Variantsnssv829297
Samples
Known GenesHEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565108
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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