A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564112



Internal ID7035212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88241750..88247662hg38UCSC Ensembl
Outerchr9:90856665..90862577hg19UCSC Ensembl
Outerchr9:90046485..90052397hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg385913
hg195913
hg185913
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006270
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564112
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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