A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701952



Internal ID15091918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105733242..106470101hg38UCSC Ensembl
Innerchr14:106199579..106926025hg19UCSC Ensembl
Innerchr14:105270624..105997070hg18UCSC Ensembl
Innerchr14:105270624..105997070hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38736860
hg19726447
hg18726447
hg17726447
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00226
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701952
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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