A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1069240



Internal ID15575740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95483436..95599660hg38UCSC Ensembl
Innerchr6:95931312..96047536hg19UCSC Ensembl
Innerchr6:96038033..96154257hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38116225
hg19116225
hg18116225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604238
Supporting Variants
Samples
Known GenesMANEA, MANEA-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1069240
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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