A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3339732



Internal ID14840002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112526038..112526086hg38UCSC Ensembl
Innerchr9:112525987..112526137hg38UCSC Ensembl
Outerchr9:112525939..112526185hg38UCSC Ensembl
chr9:115288318..115288366hg19UCSC Ensembl
Innerchr9:115288267..115288417hg19UCSC Ensembl
Outerchr9:115288219..115288465hg19UCSC Ensembl
chr9:114328139..114328187hg18UCSC Ensembl
Innerchr9:114328238..114328088hg18UCSC Ensembl
Outerchr9:114328040..114328286hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7862952, essv7862953, essv7862955
SamplesNA18520, NA18486, NA18961
Known GenesKIAA1958
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3339732
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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