A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554092



Internal ID16341501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40797556..40899833hg38UCSC Ensembl
Innerchr11:40819106..40921383hg19UCSC Ensembl
Innerchr11:40775682..40877959hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38102278
hg19102278
hg18102278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771174
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554092
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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