A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894194



Internal ID19185263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:57733441..57769290hg38UCSC Ensembl
Outerchr5:57733441..57769290hg38UCSC Ensembl
Innerchr5:57029268..57065117hg19UCSC Ensembl
Outerchr5:57029268..57065117hg19UCSC Ensembl
Innerchr5:57065025..57100874hg18UCSC Ensembl
Outerchr5:57065025..57100874hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3835850
hg1935850
hg1835850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786183
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894194
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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