A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657259



Internal ID9923364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61881337..61882148hg38UCSC Ensembl
chr2:62108472..62109283hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6026446, essv5517362, essv5984715, essv6578747
SamplesNA18530, HG00464, HG00607, HG00662
Known GenesCCT4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657259
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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