A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801147



Internal ID18829100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485135..69504046hg38UCSC Ensembl
Innerchr9:72100051..72118962hg19UCSC Ensembl
Innerchr9:71289871..71308782hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3818912
hg1918912
hg1818912
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 HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801147
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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