A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517773



Internal ID15445066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156383446..156396068hg38UCSC Ensembl
Innerchr4:157304598..157317220hg19UCSC Ensembl
Innerchr4:157524048..157536670hg18UCSC Ensembl
Innerchr4:157662203..157674825hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3812623
hg1912623
hg1812623
hg1712623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv673928, nssv661498, nssv657723, nssv681651, nssv681702, nssv654830, nssv663428, nssv670761, nssv663326, nssv669976, nssv664615, nssv654229, nssv665296, nssv668884, nssv663583, nssv656808, nssv666302, nssv667663, nssv674724, nssv669346, nssv653792, nssv690554, nssv673093, nssv682384, nssv655269, nssv674006, nssv675528, nssv672451, nssv667642, nssv684837, nssv673831, nssv660232, nssv689046, nssv657764, nssv660342, nssv651720, nssv679957, nssv664690, nssv652078, nssv687370, nssv668413, nssv665338, nssv676784, nssv653153, nssv691681
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517773
Frequency
Sample Size2026
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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