A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893969



Internal ID19184823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81906906..81984225hg38UCSC Ensembl
Outerchr4:81906906..81984225hg38UCSC Ensembl
Innerchr4:82828059..82905378hg19UCSC Ensembl
Outerchr4:82828059..82905378hg19UCSC Ensembl
Innerchr4:83047083..83124402hg18UCSC Ensembl
Outerchr4:83047083..83124402hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3877320
hg1977320
hg1877320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799532
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893969
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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