A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528891



Internal ID15456184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:182333508..182350196hg38UCSC Ensembl
Innerchr4:183254661..183271349hg19UCSC Ensembl
Innerchr4:183491655..183508343hg18UCSC Ensembl
Innerchr4:183629810..183646498hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3816689
hg1916689
hg1816689
hg1716689
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705575
Samples
Known GenesTENM3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528891
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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