A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527505



Internal ID15454798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:101380461..101386186hg38UCSC Ensembl
Innerchr12:101774239..101779964hg19UCSC Ensembl
Innerchr12:100298370..100304095hg18UCSC Ensembl
Innerchr12:100276707..100282432hg17UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg385726
hg195726
hg185726
hg175726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703957
Samples
Known GenesUTP20
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527505
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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