A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670561



Internal ID9589980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150307031..150307088hg38UCSC Ensembl
chr5:149686594..149686651hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6277886, essv5453085, essv6020957
SamplesNA12155, NA19239, NA19108
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670561
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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