A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3563865



Internal ID7034965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:107270728..107273227hg38UCSC Ensembl
Outerchr9:110033009..110035508hg19UCSC Ensembl
Outerchr9:109072830..109075329hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382500
hg192500
hg182500
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv998754
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3563865
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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