A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786758



Internal ID19160356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6064103..6080387hg38UCSC Ensembl
Innerchr9:6064103..6080387hg19UCSC Ensembl
Innerchr9:6054103..6070387hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3816285
hg1916285
hg1816285
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891540
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786758
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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