A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998081



Internal ID7081484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90295387..90295387hg38UCSC Ensembl
chr13:90947641..90947641hg19UCSC Ensembl
chr13:89745642..89745642hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38322
hg19322
hg18322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3577050
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998081
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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