A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573484



Internal ID16360893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85269021..85276284hg38UCSC Ensembl
Innerchr16:85302627..85309890hg19UCSC Ensembl
Innerchr16:83860128..83867391hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg387264
hg197264
hg187264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5272n54
Supporting Variantsnssv862247
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573484
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