A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651780



Internal ID15099477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16322892..16323589hg38UCSC Ensembl
Innerchr10:16322892..16323589hg38UCSC Ensembl
Outerchr10:16322853..16323628hg38UCSC Ensembl
chr10:16364891..16365588hg19UCSC Ensembl
Innerchr10:16364891..16365588hg19UCSC Ensembl
Outerchr10:16364852..16365627hg19UCSC Ensembl
chr10:16404897..16405594hg18UCSC Ensembl
Innerchr10:16404897..16405594hg18UCSC Ensembl
Outerchr10:16404858..16405633hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38698
hg19698
hg18698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3430008
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651780
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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