A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573609



Internal ID16014332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88534417..88547875hg38UCSC Ensembl
Innerchr16:88600825..88614283hg19UCSC Ensembl
Innerchr16:87128326..87141784hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3813459
hg1913459
hg1813459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5296n54
Supporting Variantsnssv862593, nssv862592
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573609
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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