A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526628



Internal ID15453921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47143555..47146703hg38UCSC Ensembl
Innerchr11:47165106..47168254hg19UCSC Ensembl
Innerchr11:47121682..47124830hg18UCSC Ensembl
Innerchr11:47121682..47124830hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383149
hg193149
hg183149
hg173149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702950
Samples
Known GenesC11orf49
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526628
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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