A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572852



Internal ID16360261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62225701..62338587hg38UCSC Ensembl
Innerchr16:62259605..62372491hg19UCSC Ensembl
Innerchr16:60817106..60929992hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38112887
hg19112887
hg18112887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858921
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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