A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796336



Internal ID18816636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485202..69500795hg38UCSC Ensembl
Innerchr9:72100118..72115711hg19UCSC Ensembl
Innerchr9:71289938..71305531hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3815594
hg1915594
hg1815594
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891680
Supporting Variants
Samples
Known GenesAPBA1
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796336
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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