A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691669



Internal ID15081635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105605979..106470101hg38UCSC Ensembl
Innerchr14:106072316..106926025hg19UCSC Ensembl
Innerchr14:105143361..105997070hg18UCSC Ensembl
Innerchr14:105143361..105997070hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38864123
hg19853710
hg18853710
hg17853710
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesADAM6, ELK2AP, KIAA0125, LINC00226, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691669
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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