A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565732



Internal ID16006455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99522709..99574045hg38UCSC Ensembl
Innerchr14:99989046..100040382hg19UCSC Ensembl
Innerchr14:99058799..99110135hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3851337
hg1951337
hg1851337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148974
SamplesHGDP00706
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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