A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564813



Internal ID7035913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:5638936..5644891hg38UCSC Ensembl
Outerchr9:5638936..5644891hg19UCSC Ensembl
Outerchr9:5628936..5634891hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg385956
hg195956
hg185956
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv995651
Supporting Variants
SamplesHuRef
Known GenesKIAA1432
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564813
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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