A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797097



Internal ID18827682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6650885..6697127hg38UCSC Ensembl
Innerchr9:6650885..6697127hg19UCSC Ensembl
Innerchr9:6640885..6687127hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3846243
hg1946243
hg1846243
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891541
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797097
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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