A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564322



Internal ID16351731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35533726..35534787hg38UCSC Ensembl
Innerchr14:36002932..36003993hg19UCSC Ensembl
Innerchr14:35072683..35073744hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381062
hg191062
hg181062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825729
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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