A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893999



Internal ID19184853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102657480..102727789hg38UCSC Ensembl
Outerchr4:102640552..102730224hg38UCSC Ensembl
Innerchr4:103578637..103648946hg19UCSC Ensembl
Outerchr4:103561709..103651381hg19UCSC Ensembl
Innerchr4:103797685..103867990hg18UCSC Ensembl
Outerchr4:103780757..103870425hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3889673
hg1989673
hg1889669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799536, essv25780611
Samples
Known GenesMANBA
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893999
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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