A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573072



Internal ID16360481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76684867..76734475hg38UCSC Ensembl
Innerchr16:76718764..76768372hg19UCSC Ensembl
Innerchr16:75276265..75325873hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3849609
hg1949609
hg1849609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv860447
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573072
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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