A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694595



Internal ID15084561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64502624..64528976hg38UCSC Ensembl
Innerchr14:64969342..64995694hg19UCSC Ensembl
Innerchr14:64039095..64065447hg18UCSC Ensembl
Innerchr14:64039095..64065447hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3826353
hg1926353
hg1826353
hg1726353
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521823
Supporting Variants
Samples
Known GenesZBTB1, ZBTB25
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694595
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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