A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894003



Internal ID18838171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109617846..109642294hg38UCSC Ensembl
Outerchr4:109617846..109642294hg38UCSC Ensembl
Innerchr4:110539002..110563450hg19UCSC Ensembl
Outerchr4:110539002..110563450hg19UCSC Ensembl
Innerchr4:110758451..110782899hg18UCSC Ensembl
Outerchr4:110758451..110782899hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3824449
hg1924449
hg1824449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25780742
Samples
Known GenesCCDC109B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894003
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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