A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894070



Internal ID19184924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171075081..171265209hg38UCSC Ensembl
Outerchr4:171075081..171265209hg38UCSC Ensembl
Innerchr4:171996232..172186360hg19UCSC Ensembl
Outerchr4:171996232..172186360hg19UCSC Ensembl
Innerchr4:172232807..172422935hg18UCSC Ensembl
Outerchr4:172232807..172422935hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38190129
hg19190129
hg18190129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788923
Samples
Known GenesMIR6082
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894070
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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