A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668543



Internal ID9587962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178226337..178233690hg38UCSC Ensembl
Outerchr5:178226303..178233725hg38UCSC Ensembl
Innerchr5:177653338..177660691hg19UCSC Ensembl
Outerchr5:177653304..177660726hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387423
hg197423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1060e199
Supporting Variantsessv6043668
SamplesHG00274
Known GenesPHYKPL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668543
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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