A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799453



Internal ID19178442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113986227..114033908hg38UCSC Ensembl
Innerchr5:113321924..113369605hg19UCSC Ensembl
Innerchr5:113349823..113397504hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3847682
hg1947682
hg1847682
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890712
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799453
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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