A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695997



Internal ID15085963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105708865..106489875hg38UCSC Ensembl
Innerchr14:106175202..106945882hg19UCSC Ensembl
Innerchr14:105246247..106016927hg18UCSC Ensembl
Innerchr14:105246247..106016927hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38781011
hg19770681
hg18770681
hg17770681
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesADAM6, KIAA0125, LINC00221, LINC00226
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695997
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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