A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785463



Internal ID18835603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:129234668..129241234hg38UCSC Ensembl
Innerchr9:131996947..132003513hg19UCSC Ensembl
Innerchr9:131036768..131043334hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg386567
hg196567
hg186567
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891728
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785463
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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