A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668959



Internal ID9588378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96433315..96434572hg38UCSC Ensembl
chr13:97085569..97086826hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381258
hg191258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5875031
SamplesNA19064
Known GenesHS6ST3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668959
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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