A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799708



Internal ID19169050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85764650..85841267hg38UCSC Ensembl
Innerchr6:86474368..86550985hg19UCSC Ensembl
Innerchr6:86531087..86607704hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3876618
hg1976618
hg1876618
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890898
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799708
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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