A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780742



Internal ID18822056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:109617846..109642294hg38UCSC Ensembl
Innerchr4:110539002..110563450hg19UCSC Ensembl
Innerchr4:110758451..110782899hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3824449
hg1924449
hg1824449
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894003
Supporting Variants
Samples
Known GenesCCDC109B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780742
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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