A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565998



Internal ID16353407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521722..103522656hg38UCSC Ensembl
Innerchr14:103988059..103988993hg19UCSC Ensembl
Innerchr14:103057812..103058746hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38935
hg19935
hg18935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834354, nssv834355
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565998
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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