A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789997



Internal ID19180098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91529353..91632058hg38UCSC Ensembl
Innerchr6:92239071..92341776hg19UCSC Ensembl
Innerchr6:92295792..92398497hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38102706
hg19102706
hg18102706
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890905
Supporting Variants
Samples
Known GenesCASC6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789997
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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