A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651787



Internal ID15099664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60468896..60469801hg38UCSC Ensembl
Innerchr10:60468896..60469801hg38UCSC Ensembl
Outerchr10:60467783..60469964hg38UCSC Ensembl
chr10:62228654..62229559hg19UCSC Ensembl
Innerchr10:62228654..62229559hg19UCSC Ensembl
Outerchr10:62227541..62229722hg19UCSC Ensembl
chr10:61898660..61899565hg18UCSC Ensembl
Innerchr10:61898660..61899565hg18UCSC Ensembl
Outerchr10:61897547..61899728hg18UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38906
hg19906
hg18906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3335023
Supporting Variants
SamplesNA19240
Known GenesANK3
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651787
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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