A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893922



Internal ID19184776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:53220929..53274249hg38UCSC Ensembl
Outerchr4:53220929..53274249hg38UCSC Ensembl
Innerchr4:54087096..54140416hg19UCSC Ensembl
Outerchr4:54087096..54140416hg19UCSC Ensembl
Innerchr4:53781853..53835173hg18UCSC Ensembl
Outerchr4:53781853..53835173hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3853321
hg1953321
hg1853321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800864
Samples
Known GenesSCFD2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893922
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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