A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519011



Internal ID15446304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66083757..66121925hg38UCSC Ensembl
Innerchr4:66949475..66987643hg19UCSC Ensembl
Innerchr4:66632070..66670238hg18UCSC Ensembl
Innerchr4:66778241..66816409hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3838169
hg1938169
hg1838169
hg1738169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694297
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519011
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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