A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572952



Internal ID16360361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72057644..72059235hg38UCSC Ensembl
Innerchr16:72091543..72093134hg19UCSC Ensembl
Innerchr16:70649044..70650635hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg381592
hg191592
hg181592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5186n54
Supporting Variantsnssv859125
Samples
Known GenesHP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572952
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