A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1005607



Internal ID6717727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91797298..91797596hg38UCSC Ensembl
chr9:94559580..94559878hg19UCSC Ensembl
chr9:93599401..93599699hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38299
hg19299
hg18299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3577681
SamplesHuRef
Known GenesROR2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1005607
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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