A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565751



Internal ID16006474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99603186..99609119hg38UCSC Ensembl
Innerchr14:100069523..100075456hg19UCSC Ensembl
Innerchr14:99139276..99145209hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385934
hg195934
hg185934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3891n54
Supporting Variantsnssv833029
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565751
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