A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671259



Internal ID15061225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105671130..106470101hg38UCSC Ensembl
Innerchr14:106137467..106926025hg19UCSC Ensembl
Innerchr14:105208512..105997070hg18UCSC Ensembl
Innerchr14:105208512..105997070hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38798972
hg19788559
hg18788559
hg17788559
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
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671259
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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