A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519710



Internal ID15447003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99616981..99683165hg38UCSC Ensembl
Innerchr14:100083318..100149502hg19UCSC Ensembl
Innerchr14:99153071..99219255hg18UCSC Ensembl
Innerchr14:99153071..99219255hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3866185
hg1966185
hg1866185
hg1766185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684824, nssv657762, nssv674161, nssv661143, nssv681461, nssv699972
Samples
Known GenesHHIPL1, MIR5698
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519710
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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