A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670065



Internal ID15060031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104697195..104810872hg38UCSC Ensembl
Innerchr14:105163532..105277209hg19UCSC Ensembl
Innerchr14:104234577..104348254hg18UCSC Ensembl
Innerchr14:104234577..104348254hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38113678
hg19113678
hg18113678
hg17113678
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517038
Supporting Variants
Samples
Known GenesADSSL1, AKT1, INF2, SIVA1, ZBTB42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670065
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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