A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1009938



Internal ID6722030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144531237..144531361hg38UCSC Ensembl
chr8:145756621..145756745hg19UCSC Ensembl
chr8:145727429..145727553hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38125
hg19125
hg18125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3575886
SamplesHuRef
Known GenesARHGAP39
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1009938
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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