A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526138



Internal ID15106745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:106974102..106976474hg38UCSC Ensembl
Innerchr12:107367880..107370252hg19UCSC Ensembl
Innerchr12:105892010..105894382hg18UCSC Ensembl
Innerchr12:105870347..105872719hg17UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg382373
hg192373
hg182373
hg172373
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702393
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526138
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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