A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3326698



Internal ID15173681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42639165..42644663hg38UCSC Ensembl
Innerchr9:42640165..42643663hg38UCSC Ensembl
Outerchr9:42638165..42645663hg38UCSC Ensembl
chr9:44326456..44331954hg19UCSC Ensembl
Innerchr9:44327456..44330954hg19UCSC Ensembl
Outerchr9:44325456..44332954hg19UCSC Ensembl
chr9:44266452..44271950hg18UCSC Ensembl
Innerchr9:44267452..44270950hg18UCSC Ensembl
Outerchr9:44265452..44272950hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg385499
hg195499
hg185499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4355e59
Supporting Variantsessv8696851
SamplesNA12891
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3326698
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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