A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7864963



Internal ID12970964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110964298..110964299hg38UCSC Ensembl
Innerchr9:110964294..110964303hg38UCSC Ensembl
Outerchr9:110964293..110964304hg38UCSC Ensembl
chr9:113726578..113726579hg19UCSC Ensembl
Innerchr9:113726574..113726583hg19UCSC Ensembl
Outerchr9:113726573..113726584hg19UCSC Ensembl
chr9:112766399..112766400hg18UCSC Ensembl
Innerchr9:112766404..112766395hg18UCSC Ensembl
Outerchr9:112766394..112766405hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3855
hg1955
hg1855
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3445715
Supporting Variants
SamplesNA12005
Known GenesLPAR1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7864963
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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