A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796441



Internal ID19175070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25509547..25576546hg38UCSC Ensembl
Innerchr9:25509545..25576544hg19UCSC Ensembl
Innerchr9:25499545..25566544hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3867000
hg1967000
hg1867000
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891643
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796441
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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