A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522639



Internal ID15449932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:115098361..115107151hg38UCSC Ensembl
Innerchr12:115536166..115544956hg19UCSC Ensembl
Innerchr12:114020549..114029339hg18UCSC Ensembl
Innerchr12:113998886..114007676hg17UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg388791
hg198791
hg188791
hg178791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706037
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522639
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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