A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796477



Internal ID19181456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70365524..70382338hg38UCSC Ensembl
Innerchr4:71231241..71248055hg19UCSC Ensembl
Innerchr4:71265830..71282644hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3816815
hg1916815
hg1816815
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893960
Supporting Variants
Samples
Known GenesSMR3A
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796477
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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