A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176190



Internal ID15533365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85977166..86046547hg38UCSC Ensembl
Innerchr11:85688209..85757589hg19UCSC Ensembl
Innerchr11:85365857..85435237hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3869382
hg1969381
hg1869381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555643
Supporting Variants
SamplesNINDS_147
Known GenesPICALM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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