A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798046



Internal ID18832601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65768587..65900124hg38UCSC Ensembl
Innerchr6:66478480..66610017hg19UCSC Ensembl
Innerchr6:66535201..66666738hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38131538
hg19131538
hg18131538
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890869
Supporting Variants
Samples
Known GenesSLC25A51P1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=33
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798046
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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