A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8651766



Internal ID15099460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101855054..101855391hg38UCSC Ensembl
Innerchr10:101855054..101855391hg38UCSC Ensembl
Outerchr10:101854019..101857068hg38UCSC Ensembl
chr10:103614811..103615148hg19UCSC Ensembl
Innerchr10:103614811..103615148hg19UCSC Ensembl
Outerchr10:103613776..103616825hg19UCSC Ensembl
chr10:103604801..103605138hg18UCSC Ensembl
Innerchr10:103604801..103605138hg18UCSC Ensembl
Outerchr10:103603766..103606815hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38338
hg19338
hg18338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3450028
Supporting Variants
SamplesNA19240
Known GenesC10orf76
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8651766
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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