A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516251



Internal ID15443544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152135395..152163567hg38UCSC Ensembl
Innerchr5:151514956..151543128hg19UCSC Ensembl
Innerchr5:151495149..151523321hg18UCSC Ensembl
Innerchr5:151495149..151523321hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3828173
hg1928173
hg1828173
hg1728173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684913, nssv670292, nssv671970, nssv671194, nssv657752, nssv652225, nssv661990, nssv677224, nssv677704, nssv681757, nssv670105, nssv651724, nssv666598, nssv688130, nssv661659, nssv689429, nssv655191, nssv663051, nssv656619, nssv674282, nssv655514, nssv654922, nssv665103, nssv667804, nssv669284, nssv674595, nssv684941, nssv665594, nssv652805, nssv664677, nssv665878, nssv662436, nssv685748, nssv679507, nssv663083, nssv671378, nssv691169, nssv658844, nssv676163, nssv665310, nssv663785, nssv658954, nssv690199, nssv674571, nssv671273, nssv652675, nssv671662, nssv680680, nssv686371, nssv676620, nssv665956, nssv658477, nssv691529, nssv673244, nssv653165, nssv676814, nssv678333, nssv654785, nssv691000, nssv654014, nssv656172, nssv687228, nssv670594, nssv670325
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516251
Frequency
Sample Size2026
Observed Gain0
Observed Loss64
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer