A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894053



Internal ID19184907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152063163..152085160hg38UCSC Ensembl
Outerchr4:152063163..152085160hg38UCSC Ensembl
Innerchr4:152984315..153006312hg19UCSC Ensembl
Outerchr4:152984315..153006312hg19UCSC Ensembl
Innerchr4:153203765..153225762hg18UCSC Ensembl
Outerchr4:153203765..153225762hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3821998
hg1921998
hg1821998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25783031
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894053
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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