A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565127



Internal ID16005850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73532494..73557222hg38UCSC Ensembl
Innerchr14:73999198..74023926hg19UCSC Ensembl
Innerchr14:73068951..73093679hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3824729
hg1924729
hg1824729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3766n54
Supporting Variantsnssv829328, nssv829329
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565127
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer