A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528900



Internal ID15456193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108688384..108706869hg38UCSC Ensembl
Innerchr4:109609540..109628025hg19UCSC Ensembl
Innerchr4:109828989..109847474hg18UCSC Ensembl
Innerchr4:109967144..109985629hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3818486
hg1918486
hg1818486
hg1718486
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705584
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528900
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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