A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696969



Internal ID15086935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70068106..70074309hg38UCSC Ensembl
Innerchr14:70534823..70541026hg19UCSC Ensembl
Innerchr14:69604576..69610779hg18UCSC Ensembl
Innerchr14:69604576..69610779hg17UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg386204
hg196204
hg186204
hg176204
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519644
Supporting Variants
Samples
Known GenesSLC8A3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696969
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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