A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788395



Internal ID19167738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61119609..61328788hg38UCSC Ensembl
Innerchr6:61908413..62118105hg19UCSC Ensembl
Innerchr6:61966372..62176064hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38209180
hg19209693
hg18209693
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890857
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788395
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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