A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572828



Internal ID16360237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58944346..58976597hg38UCSC Ensembl
Innerchr16:58978250..59010501hg19UCSC Ensembl
Innerchr16:57535751..57568002hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3832252
hg1932252
hg1832252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858902
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572828
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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