A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9313n54



Internal ID20142737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150959225..150963161hg38UCSC Ensembl
chr4:151880377..151884313hg19UCSC Ensembl
chr4:152099827..152103763hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383937
hg193937
hg183937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595698, nsv595694
Samples
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9313n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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