A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657042



Internal ID15047008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104080556..104191423hg38UCSC Ensembl
Innerchr14:104546893..104657760hg19UCSC Ensembl
Innerchr14:103616646..103727513hg18UCSC Ensembl
Innerchr14:103616646..103727513hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38110868
hg19110868
hg18110868
hg17110868
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519605
Supporting Variants
Samples
Known GenesASPG, KIF26A, MIR203, MIR3545
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657042
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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