A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572839



Internal ID16360248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60880161..60945907hg38UCSC Ensembl
Innerchr16:60914065..60979811hg19UCSC Ensembl
Innerchr16:59471566..59537312hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3865747
hg1965747
hg1865747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv858911
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572839
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer