A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691845



Internal ID15081811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104793397..104801891hg38UCSC Ensembl
Innerchr14:105259734..105268228hg19UCSC Ensembl
Innerchr14:104330779..104339273hg18UCSC Ensembl
Innerchr14:104330779..104339273hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg388495
hg198495
hg188495
hg178495
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517038
Supporting Variants
Samples
Known GenesAKT1, ZBTB42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691845
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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