A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780233



Internal ID19169196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144510219..144797128hg38UCSC Ensembl
Innerchr6:144831355..145118264hg19UCSC Ensembl
Innerchr6:144873048..145159957hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38286910
hg19286910
hg18286910
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890960
Supporting Variants
Samples
Known GenesUTRN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=61
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780233
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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