A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572565



Internal ID16359974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48475400..48485279hg38UCSC Ensembl
Innerchr16:48509311..48519190hg19UCSC Ensembl
Innerchr16:47066812..47076691hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg389880
hg199880
hg189880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv857185
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572565
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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