A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893937



Internal ID19184791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64759003..65042298hg38UCSC Ensembl
Outerchr4:64759003..65042298hg38UCSC Ensembl
Innerchr4:65624721..65908016hg19UCSC Ensembl
Outerchr4:65624721..65908016hg19UCSC Ensembl
Innerchr4:65307316..65590611hg18UCSC Ensembl
Outerchr4:65307316..65590611hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38283296
hg19283296
hg18283296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781220
Samples
Known GenesLOC401134
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893937
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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