A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5437n100



Internal ID20157053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150947676..150963136hg38UCSC Ensembl
chr4:151868828..151884288hg19UCSC Ensembl
chr4:152088278..152103738hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3815461
hg1915461
hg1815461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034558, nsv1026672
Samples
Known GenesLRBA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5437n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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