A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605836



Internal ID6646080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95706463..95713774hg38UCSC Ensembl
Innerchr5:95706963..95713274hg38UCSC Ensembl
Outerchr5:95705463..95714774hg38UCSC Ensembl
chr5:95042167..95049478hg19UCSC Ensembl
Innerchr5:95042667..95048978hg19UCSC Ensembl
Outerchr5:95041167..95050478hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg387312
hg197312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1112e214
Supporting Variantsessv11983053, essv11983054, essv11983055, essv11983052, essv11983056
SamplesHG01815, NA19717, HG02408, HG01804, HG02462
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605836
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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