A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524524



Internal ID15105131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:108878275..108899544hg38UCSC Ensembl
Innerchr12:109272051..109293320hg19UCSC Ensembl
Innerchr12:107796180..107817449hg18UCSC Ensembl
Innerchr12:107774517..107795786hg17UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg3821270
hg1921270
hg1821270
hg1721270
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700473
Samples
Known GenesDAO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524524
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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