A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3574826



Internal ID6699522
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989139
Supporting Variants
SamplesHuRef
Known GenesROBO2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3574826
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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