A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893891



Internal ID19184711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18933277..19040735hg38UCSC Ensembl
Outerchr4:18933277..19040735hg38UCSC Ensembl
Innerchr4:18934900..19042358hg19UCSC Ensembl
Outerchr4:18934900..19042358hg19UCSC Ensembl
Innerchr4:18543998..18651456hg18UCSC Ensembl
Outerchr4:18543998..18651456hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38107459
hg19107459
hg18107459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799215
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893891
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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