A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573370



Internal ID16360779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82131578..82151715hg38UCSC Ensembl
Innerchr16:82165183..82185320hg19UCSC Ensembl
Innerchr16:80722684..80742821hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3820138
hg1920138
hg1820138
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5252n54
Supporting Variantsnssv861946
Samples
Known GenesMPHOSPH6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573370
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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