A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673945



Internal ID15063911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105585696..105671130hg38UCSC Ensembl
Innerchr14:106052033..106137467hg19UCSC Ensembl
Innerchr14:105123078..105208512hg18UCSC Ensembl
Innerchr14:105123078..105208512hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3885435
hg1985435
hg1885435
hg1785435
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673945
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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