A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660990



Internal ID9580409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76353962..76356512hg38UCSC Ensembl
chr10:78113720..78116270hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg382551
hg192551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6017846, essv5545073
SamplesHG00698, HG00559
Known GenesC10orf11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660990
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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