A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792507



Internal ID19170104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:84722520..84816106hg38UCSC Ensembl
Innerchr5:84018338..84111924hg19UCSC Ensembl
Innerchr5:84054094..84147680hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3893587
hg1993587
hg1893587
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890666
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=18
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792507
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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