A curated catalogue of human genomic structural variation




Variant Details

Variant: esv989139



Internal ID6725109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77295556..77295661hg38UCSC Ensembl
chr3:77344707..77344812hg19UCSC Ensembl
chr3:77427397..77427502hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38106
hg19106
hg18106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3574826
SamplesHuRef
Known GenesROBO2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv989139
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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