A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524439



Internal ID15105046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:106959817..106974102hg38UCSC Ensembl
Innerchr12:107353595..107367880hg19UCSC Ensembl
Innerchr12:105877725..105892010hg18UCSC Ensembl
Innerchr12:105856062..105870347hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3814286
hg1914286
hg1814286
hg1714286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv99n21
Supporting Variantsnssv700370
Samples
Known GenesC12orf23
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524439
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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