A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565444



Internal ID6690140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:86998975..86999261hg38UCSC Ensembl
Outerchr9:89613890..89614176hg19UCSC Ensembl
Outerchr9:88803710..88803996hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382800
hg192800
hg182800
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994498
Supporting Variants
SamplesHuRef
Known GenesLOC100506834
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565444
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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