A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6144843



Internal ID8937834
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 Flag1
Merged StatusS
Merged Variantsesv2665275
Supporting Variants
SamplesHG00463
Known GenesLINC00359
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6144843
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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