A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527189



Internal ID15107796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2243138..2276689hg38UCSC Ensembl
Innerchr4:2244865..2278416hg19UCSC Ensembl
Innerchr4:2214663..2248214hg18UCSC Ensembl
Innerchr4:2212096..2245647hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3833552
hg1933552
hg1833552
hg1733552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703586
Samples
Known GenesMIR4800, MXD4, ZFYVE28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527189
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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