A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785951



Internal ID19180402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97162322..97195269hg38UCSC Ensembl
Innerchr9:99924604..99957551hg19UCSC Ensembl
Innerchr9:98964425..98997372hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3832948
hg1932948
hg1832948
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891695
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785951
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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