A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998986



Internal ID48576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:73355117..73357249hg38UCSC Ensembl
Outerchr15:73647458..73649590hg19UCSC Ensembl
Outerchr15:71434511..71436643hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382815
hg192815
hg182815
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565790
SamplesHuRef
Known GenesHCN4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998986
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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