A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893876



Internal ID18838010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10345427..10660766hg38UCSC Ensembl
Outerchr4:10345427..10660766hg38UCSC Ensembl
Innerchr4:10347051..10662390hg19UCSC Ensembl
Outerchr4:10347051..10662390hg19UCSC Ensembl
Innerchr4:9956149..10271488hg18UCSC Ensembl
Outerchr4:9956149..10271488hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38315340
hg19315340
hg18315340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789951
Samples
Known GenesCLNK, ZNF518B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893876
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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