A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573757



Internal ID16361166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89830015..89831885hg38UCSC Ensembl
Innerchr16:89896423..89898293hg19UCSC Ensembl
Innerchr16:88423924..88425794hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381871
hg191871
hg181871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5327n54
Supporting Variantsnssv863398, nssv863394, nssv863408, nssv863407, nssv863399, nssv863402, nssv863401, nssv863392, nssv863386, nssv863389, nssv863395, nssv863396, nssv863406, nssv863404, nssv863393, nssv863397, nssv863409, nssv863390, nssv863387, nssv863391, nssv863400, nssv863405, nssv863388, nssv863403
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573757
Frequency
Sample Size17421
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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