A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779819



Internal ID19176137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:22746735..22809848hg38UCSC Ensembl
Innerchr9:22746734..22809847hg19UCSC Ensembl
Innerchr9:22736734..22799847hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3863114
hg1963114
hg1863114
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891635
Supporting Variants
Samples
Known GenesFLJ35282
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779819
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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