A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3577681



Internal ID6702377
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 StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1005607
Supporting Variants
SamplesHuRef
Known GenesROR2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3577681
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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