A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573603



Internal ID16014326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533696..88534469hg38UCSC Ensembl
Innerchr16:88600104..88600877hg19UCSC Ensembl
Innerchr16:87127605..87128378hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38774
hg19774
hg18774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5297n54
Supporting Variantsnssv862585, nssv862582, nssv862583, nssv862581, nssv862584
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573603
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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