A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3425626



Internal ID15272583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95837692..95839190hg38UCSC Ensembl
Innerchr5:95838190..95838692hg38UCSC Ensembl
Outerchr5:95836692..95840190hg38UCSC Ensembl
chr5:95173396..95174894hg19UCSC Ensembl
Innerchr5:95173894..95174396hg19UCSC Ensembl
Outerchr5:95172396..95175894hg19UCSC Ensembl
chr5:95199152..95200650hg18UCSC Ensembl
Innerchr5:95200152..95199650hg18UCSC Ensembl
Outerchr5:95198152..95201650hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg381499
hg191499
hg181499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8695001
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3425626
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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