A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663465



Internal ID9929570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161564209..161564682hg38UCSC Ensembl
chr5:160991215..160991688hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5567954, essv6401709, essv6500892, essv6444103, essv5748351
SamplesNA19703, NA19313, NA19137, NA19451, HG01082
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663465
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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