A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572356



Internal ID16359765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34939284..34956323hg38UCSC Ensembl
Innerchr16:34173678..34190694hg19UCSC Ensembl
Innerchr16:34031179..34048195hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3817040
hg1917017
hg1817017
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5081n54
Supporting Variantsnssv856195, nssv856197, nssv856196, nssv856194
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572356
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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