A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553565



Internal ID15994288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16198743..16286154hg38UCSC Ensembl
Innerchr11:16220289..16307700hg19UCSC Ensembl
Innerchr11:16176865..16264276hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3887412
hg1987412
hg1887412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768279
Samples
Known GenesSOX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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