A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572886



Internal ID16360295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63053302..63087176hg38UCSC Ensembl
Innerchr16:63087206..63121080hg19UCSC Ensembl
Innerchr16:61644707..61678581hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3833875
hg1933875
hg1833875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5176n54
Supporting Variantsnssv859058
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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