A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564487



Internal ID7035587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:97954577..97956504hg38UCSC Ensembl
Outerchr13:98606831..98608758hg19UCSC Ensembl
Outerchr13:97404832..97406759hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg385470
hg195470
hg185470
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006772
Supporting Variants
SamplesHuRef
Known GenesIPO5
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564487
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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