A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526969



Internal ID15454262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2243138..2301372hg38UCSC Ensembl
Innerchr4:2244865..2303099hg19UCSC Ensembl
Innerchr4:2214663..2272897hg18UCSC Ensembl
Innerchr4:2212096..2270330hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3858235
hg1958235
hg1858235
hg1758235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv312n21
Supporting Variantsnssv703341
Samples
Known GenesMIR4800, MXD4, ZFYVE28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526969
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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