A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565182



Internal ID16005905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:74220714..74299190hg38UCSC Ensembl
Innerchr14:74687417..74765893hg19UCSC Ensembl
Innerchr14:73757170..73835646hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3878477
hg1978477
hg1878477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829517
Samples
Known GenesABCD4, VSX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565182
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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