A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671972



Internal ID9591391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160757165..160759283hg38UCSC Ensembl
Outerchr5:160757008..160759436hg38UCSC Ensembl
Innerchr5:160184172..160186290hg19UCSC Ensembl
Outerchr5:160184015..160186443hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382429
hg192429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6177463
SamplesNA19347
Known GenesATP10B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671972
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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