A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781220



Internal ID19168904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:64759003..65042298hg38UCSC Ensembl
Innerchr4:65624721..65908016hg19UCSC Ensembl
Innerchr4:65307316..65590611hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38283296
hg19283296
hg18283296
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893937
Supporting Variants
Samples
Known GenesLOC401134
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=51
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25781220
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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