A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526498



Internal ID15453791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:126426244..126441236hg38UCSC Ensembl
Innerchr4:127347399..127362391hg19UCSC Ensembl
Innerchr4:127566849..127581841hg18UCSC Ensembl
Innerchr4:127705004..127719996hg17UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3814993
hg1914993
hg1814993
hg1714993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702807
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526498
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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