A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893960



Internal ID19184814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70365524..70379312hg38UCSC Ensembl
Outerchr4:70363334..70386524hg38UCSC Ensembl
Innerchr4:71231241..71245029hg19UCSC Ensembl
Outerchr4:71229051..71252241hg19UCSC Ensembl
Innerchr4:71265830..71279618hg18UCSC Ensembl
Outerchr4:71263640..71286830hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3823191
hg1923191
hg1823191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800416, essv25801534, essv25796477, essv25800721, essv25797971, essv25784471, essv25782094, essv25801450
Samples
Known GenesSMR3A, SMR3B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893960
Frequency
Sample Size3017
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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