A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525200



Internal ID15452493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131179266..131606186hg38UCSC Ensembl
Innerchr4:132100421..132527341hg19UCSC Ensembl
Innerchr4:132319871..132746791hg18UCSC Ensembl
Innerchr4:132458026..132884946hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38426921
hg19426921
hg18426921
hg17426921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701281
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525200
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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