A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3367696



Internal ID15214672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53161405..53161424hg38UCSC Ensembl
Innerchr15:53161401..53161428hg38UCSC Ensembl
Outerchr15:53161382..53161447hg38UCSC Ensembl
chr15:53453602..53453621hg19UCSC Ensembl
Innerchr15:53453598..53453625hg19UCSC Ensembl
Outerchr15:53453579..53453644hg19UCSC Ensembl
chr15:51240894..51240913hg18UCSC Ensembl
Innerchr15:51240917..51240890hg18UCSC Ensembl
Outerchr15:51240871..51240936hg18UCSC Ensembl
Cytoband15q21.3
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 Variantsessv9668746
SamplesNA07346
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3367696
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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