A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670761



Internal ID9936866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125710948..125717560hg38UCSC Ensembl
chr10:127399517..127406129hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386613
hg196613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5561421
SamplesHG00732
Known GenesFLJ37035
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670761
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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