A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174908



Internal ID15533398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95951695..95978750hg38UCSC Ensembl
Innerchr11:95684859..95711914hg19UCSC Ensembl
Innerchr11:95324507..95351562hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3827056
hg1927056
hg1827056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555968
Supporting Variants
SamplesNINDS_152
Known GenesMAML2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174908
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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