A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005577



Internal ID7070672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135836132..135839081hg38UCSC Ensembl
Innerchr9:138727978..138730927hg19UCSC Ensembl
Innerchr9:137867799..137870748hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382950
hg192950
hg182950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587130
SamplesHuRef
Known GenesCAMSAP1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005577
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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