A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799532



Internal ID19159605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:81906906..81984225hg38UCSC Ensembl
Innerchr4:82828059..82905378hg19UCSC Ensembl
Innerchr4:83047083..83124402hg18UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg3877320
hg1977320
hg1877320
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893969
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799532
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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