A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176195



Internal ID15879313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:89011248..89108291hg38UCSC Ensembl
Innerchr11:88744416..88841459hg19UCSC Ensembl
Innerchr11:88384064..88481107hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3897044
hg1997044
hg1897044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555732
Supporting Variants
SamplesHGDP01343
Known GenesGRM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176195
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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