A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573598



Internal ID16014321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88533592..88534355hg38UCSC Ensembl
Innerchr16:88600000..88600763hg19UCSC Ensembl
Innerchr16:87127501..87128264hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38764
hg19764
hg18764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5297n54
Supporting Variantsnssv862575
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573598
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