A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796479



Internal ID19173615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:76682109..76691135hg38UCSC Ensembl
Innerchr6:77391826..77400852hg19UCSC Ensembl
Innerchr6:77448545..77457571hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg389027
hg199027
hg189027
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890885
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796479
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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