A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7773808



Internal ID13224084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79503528..79503529hg38UCSC Ensembl
Innerchr15:79503510..79503547hg38UCSC Ensembl
Outerchr15:79503509..79503548hg38UCSC Ensembl
chr15:79795870..79795871hg19UCSC Ensembl
Innerchr15:79795852..79795889hg19UCSC Ensembl
Outerchr15:79795851..79795890hg19UCSC Ensembl
chr15:77582925..77582926hg18UCSC Ensembl
Innerchr15:77582944..77582907hg18UCSC Ensembl
Outerchr15:77582906..77582945hg18UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38291
hg19291
hg18291
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3305580
Supporting Variants
SamplesNA11931
Known Genes
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7773808
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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