A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572883



Internal ID16360292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63043867..63086741hg38UCSC Ensembl
Innerchr16:63077771..63120645hg19UCSC Ensembl
Innerchr16:61635272..61678146hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3842875
hg1942875
hg1842875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5176n54
Supporting Variantsnssv1149178
Samples1798860084_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572883
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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