A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659526



Internal ID9578945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46464109..46465673hg38UCSC Ensembl
chr13:47038244..47039808hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg381565
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5555722, essv6431976, essv6355951, essv6171499, essv6215392, essv6200588, essv5851200, essv5485715, essv5942115, essv6299579
SamplesHG00613, HG00111, NA19057, NA19075, HG00640, NA18599, HG00118, HG01125, NA19381, NA18980
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659526
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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