A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572391



Internal ID16359800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35911586..35994041hg38UCSC Ensembl
Innerchr16:35145957..35228412hg19UCSC Ensembl
Innerchr16:35003458..35085913hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3882456
hg1982456
hg1882456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5086n54
Supporting Variantsnssv856266
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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