A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572841



Internal ID16360250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:61090294..61169953hg38UCSC Ensembl
Innerchr16:61124198..61203857hg19UCSC Ensembl
Innerchr16:59681699..59761358hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3879660
hg1979660
hg1879660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149174
SamplesHGDP00153
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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