A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659593



Internal ID9579012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62401859..62409805hg38UCSC Ensembl
chr5:61697686..61705632hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg387947
hg197947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1023e199
Supporting Variantsessv6506558
SamplesNA18602
Known GenesDIMT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659593
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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