A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9668903



Internal ID13604964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58877162..58877181hg38UCSC Ensembl
Innerchr15:58877158..58877185hg38UCSC Ensembl
Outerchr15:58877139..58877204hg38UCSC Ensembl
chr15:59169361..59169380hg19UCSC Ensembl
Innerchr15:59169357..59169384hg19UCSC Ensembl
Outerchr15:59169338..59169403hg19UCSC Ensembl
chr15:56956653..56956672hg18UCSC Ensembl
Innerchr15:56956676..56956649hg18UCSC Ensembl
Outerchr15:56956630..56956695hg18UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3340483
Supporting Variants
SamplesNA12814
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9668903
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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