A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8677455



Internal ID14710963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79805831..79805845hg38UCSC Ensembl
Innerchr9:79805827..79805847hg38UCSC Ensembl
Outerchr9:79805815..79805861hg38UCSC Ensembl
chr9:82420746..82420760hg19UCSC Ensembl
Innerchr9:82420742..82420762hg19UCSC Ensembl
Outerchr9:82420730..82420776hg19UCSC Ensembl
chr9:81610566..81610580hg18UCSC Ensembl
Innerchr9:81610582..81610562hg18UCSC Ensembl
Outerchr9:81610550..81610596hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38235
hg19235
hg18235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3336978
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8677455
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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