A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3402109



Internal ID14902385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109149970..109149989hg38UCSC Ensembl
Innerchr9:109149966..109149993hg38UCSC Ensembl
Outerchr9:109149947..109150012hg38UCSC Ensembl
chr9:111912250..111912269hg19UCSC Ensembl
Innerchr9:111912246..111912273hg19UCSC Ensembl
Outerchr9:111912227..111912292hg19UCSC Ensembl
chr9:110952071..110952090hg18UCSC Ensembl
Innerchr9:110952094..110952067hg18UCSC Ensembl
Outerchr9:110952048..110952113hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9644869
SamplesNA12812
Known GenesFRRS1L
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3402109
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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