A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520201



Internal ID15447494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41288424..41302863hg38UCSC Ensembl
Innerchr11:41309974..41324413hg19UCSC Ensembl
Innerchr11:41266550..41280989hg18UCSC Ensembl
Innerchr11:41266550..41280989hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3814440
hg1914440
hg1814440
hg1714440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697277
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520201
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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