A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565735



Internal ID16006458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99589385..99683165hg38UCSC Ensembl
Innerchr14:100055722..100149502hg19UCSC Ensembl
Innerchr14:99125475..99219255hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3893781
hg1993781
hg1893781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832990
Samples
Known GenesCCDC85C, HHIPL1, MIR5698
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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