A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665275



Internal ID9931380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96955492..96966051hg38UCSC Ensembl
chr13:97607746..97618305hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3810560
hg1910560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6144843
SamplesHG00463
Known GenesLINC00359
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665275
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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