A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656228



Internal ID15046194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105585696..106489875hg38UCSC Ensembl
Innerchr14:106052033..106945882hg19UCSC Ensembl
Innerchr14:105123078..106016927hg18UCSC Ensembl
Innerchr14:105123078..106016927hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38904180
hg19893850
hg18893850
hg17893850
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517055
Supporting Variants
Samples
Known GenesADAM6, ELK2AP, KIAA0125, LINC00221, LINC00226, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656228
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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