A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798044



Internal ID18814789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:12790188..13033344hg38UCSC Ensembl
Innerchr6:12790420..13033576hg19UCSC Ensembl
Innerchr6:12898406..13141562hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38243157
hg19243157
hg18243157
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890791
Supporting Variants
Samples
Known GenesPHACTR1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=39
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798044
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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