A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573755



Internal ID16361164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830015..89831767hg38UCSC Ensembl
Innerchr16:89896423..89898175hg19UCSC Ensembl
Innerchr16:88423924..88425676hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381753
hg191753
hg181753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5327n54
Supporting Variantsnssv863379, nssv863370, nssv863377, nssv863373, nssv863381, nssv863369, nssv863380, nssv863372, nssv863376, nssv863374, nssv863375, nssv863371, nssv863378
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573755
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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