A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522233



Internal ID8416508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25239348..25244348hg38UCSC Ensembl
Innerchr12:25392282..25397282hg19UCSC Ensembl
Innerchr12:25283549..25288549hg18UCSC Ensembl
Innerchr12:25283549..25288549hg17UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg385001
hg195001
hg185001
hg175001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695011
Samples
Known GenesKRAS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522233
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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