A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520884



Internal ID15448177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96061264..96065974hg38UCSC Ensembl
Innerchr14:96527601..96532311hg19UCSC Ensembl
Innerchr14:95597354..95602064hg18UCSC Ensembl
Innerchr14:95597354..95602064hg17UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg384711
hg194711
hg184711
hg174711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv680855, nssv676984
Samples
Known GenesC14orf132
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520884
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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