A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572880



Internal ID16360289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63020273..63087176hg38UCSC Ensembl
Innerchr16:63054177..63121080hg19UCSC Ensembl
Innerchr16:61611678..61678581hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3866904
hg1966904
hg1866904
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5175n54
Supporting Variantsnssv859054, nssv859053
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572880
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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