A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694158



Internal ID15430810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25974297..25996770hg38UCSC Ensembl
Innerchr12:26127230..26149703hg19UCSC Ensembl
Innerchr12:26018497..26040970hg18UCSC Ensembl
Innerchr12:26018497..26040970hg17UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3822474
hg1922474
hg1822474
hg1722474
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522351
Supporting Variants
Samples
Known GenesRASSF8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694158
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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