A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554091



Internal ID16341500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:40716749..40802758hg38UCSC Ensembl
Innerchr11:40738299..40824308hg19UCSC Ensembl
Innerchr11:40694875..40780884hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3886010
hg1986010
hg1886010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771173
Samples
Known GenesLRRC4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554091
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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