A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9314n54



Internal ID20142738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150959613..150962562hg38UCSC Ensembl
chr4:151880765..151883714hg19UCSC Ensembl
chr4:152100215..152103164hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382950
hg192950
hg182950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv595696, nsv595695, nsv595697
Samples
Known GenesLRBA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9314n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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