A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894051



Internal ID19184905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:148712561..148739759hg38UCSC Ensembl
Outerchr4:148712561..148739759hg38UCSC Ensembl
Innerchr4:149633713..149660911hg19UCSC Ensembl
Outerchr4:149633713..149660911hg19UCSC Ensembl
Innerchr4:149853163..149880361hg18UCSC Ensembl
Outerchr4:149853163..149880361hg18UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3827199
hg1927199
hg1827199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800624
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894051
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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