A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890708



Internal ID19185010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110111157..110300884hg38UCSC Ensembl
Outerchr5:110111157..110300884hg38UCSC Ensembl
Innerchr5:109446858..109636585hg19UCSC Ensembl
Outerchr5:109446858..109636585hg19UCSC Ensembl
Innerchr5:109474757..109664484hg18UCSC Ensembl
Outerchr5:109474757..109664484hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38189728
hg19189728
hg18189728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25779197
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890708
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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