A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780611



Internal ID19173928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102657480..102730224hg38UCSC Ensembl
Innerchr4:103578637..103651381hg19UCSC Ensembl
Innerchr4:103797685..103870425hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3872745
hg1972745
hg1872741
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893999
Supporting Variants
Samples
Known GenesMANBA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780611
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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