A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524627



Internal ID15451920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:64688550..64697251hg38UCSC Ensembl
Innerchr12:65082330..65091031hg19UCSC Ensembl
Innerchr12:63368597..63377298hg18UCSC Ensembl
Innerchr12:63368597..63377298hg17UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg388702
hg198702
hg188702
hg178702
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700590
Samples
Known GenesRASSF3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524627
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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