A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528259



Internal ID15455552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:73909094..73967198hg38UCSC Ensembl
Innerchr12:74302874..74360978hg19UCSC Ensembl
Innerchr12:72589141..72647245hg18UCSC Ensembl
Innerchr12:72589141..72647245hg17UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3858105
hg1958105
hg1858105
hg1758105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704825
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528259
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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