A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520229



Internal ID15447522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107778300..107799502hg38UCSC Ensembl
Innerchr11:107649026..107670228hg19UCSC Ensembl
Innerchr11:107154236..107175438hg18UCSC Ensembl
Innerchr11:107154236..107175438hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3821203
hg1921203
hg1821203
hg1721203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662039, nssv693254, nssv685596, nssv683123, nssv662617, nssv677842, nssv687797, nssv684540
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520229
Frequency
Sample Size2026
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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