A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789804



Internal ID19175579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:86265776..86747734hg38UCSC Ensembl
Innerchr6:86975494..87457452hg19UCSC Ensembl
Innerchr6:87032213..87514171hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38481959
hg19481959
hg18481959
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890899
Supporting Variants
Samples
Known GenesMIR548AD
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=84
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789804
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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