A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3310528



Internal ID15157479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:168000110..168001666hg38UCSC Ensembl
Outerchr3:168000110..168001666hg38UCSC Ensembl
Innerchr3:167717898..167719454hg19UCSC Ensembl
Outerchr3:167717898..167719454hg19UCSC Ensembl
Innerchr3:169202148..169200592hg18UCSC Ensembl
Outerchr3:169200592..169202148hg18UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg381187
hg191187
hg181187
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7843506
SamplesNA19240
Known Genes
MethodSequencing
Analysismapreads
PlatformABI SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3310528
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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