A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555975



Internal ID16343384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96269098..96275952hg38UCSC Ensembl
Innerchr11:96002262..96009116hg19UCSC Ensembl
Innerchr11:95641910..95648764hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386855
hg196855
hg186855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781628
Samples
Known GenesMAML2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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