A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658273



Internal ID9924378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135079918..135086506hg38UCSC Ensembl
Outerchr5:135079881..135086556hg38UCSC Ensembl
Innerchr5:134415608..134422196hg19UCSC Ensembl
Outerchr5:134415571..134422246hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg386676
hg196676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5467276
SamplesNA19788
Known GenesC5orf66
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658273
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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