A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573368



Internal ID16360777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82116688..82183017hg38UCSC Ensembl
Innerchr16:82150293..82216622hg19UCSC Ensembl
Innerchr16:80707794..80774123hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3866330
hg1966330
hg1866330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5251n54
Supporting Variantsnssv861944
Samples
Known GenesMPHOSPH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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