A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782284



Internal ID19165743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101796603..101882777hg38UCSC Ensembl
Innerchr9:104558885..104645059hg19UCSC Ensembl
Innerchr9:103598706..103684880hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3886175
hg1986175
hg1886175
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891697
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782284
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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