A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697166



Internal ID15103665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63849498..63901896hg38UCSC Ensembl
Innerchr9:63850498..63900896hg38UCSC Ensembl
Outerchr9:63848498..63902896hg38UCSC Ensembl
chr9:68445232..68497630hg19UCSC Ensembl
Innerchr9:68446232..68496630hg19UCSC Ensembl
Outerchr9:68444232..68498630hg19UCSC Ensembl
chr9:67935052..67987450hg18UCSC Ensembl
Innerchr9:67936052..67986450hg18UCSC Ensembl
Outerchr9:67934052..67988450hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3852399
hg1952399
hg1852399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3441343
Supporting Variants
SamplesNA19240
Known GenesLOC642236
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697166
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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