A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555970



Internal ID16343379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96219500..96244506hg38UCSC Ensembl
Innerchr11:95952664..95977670hg19UCSC Ensembl
Innerchr11:95592312..95617318hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3825007
hg1925007
hg1825007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174909
SamplesNINDS_67
Known GenesMAML2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555970
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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