A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890765



Internal ID19185067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:165621296..165772598hg38UCSC Ensembl
Outerchr5:165621296..165772598hg38UCSC Ensembl
Innerchr5:165048301..165199603hg19UCSC Ensembl
Outerchr5:165048301..165199603hg19UCSC Ensembl
Innerchr5:164980879..165132181hg18UCSC Ensembl
Outerchr5:164980879..165132181hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38151303
hg19151303
hg18151303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25793028
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890765
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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