A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862306



Internal ID15809576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85680640..85703265hg38UCSC Ensembl
Innerchr16:85714246..85736871hg19UCSC Ensembl
Innerchr16:84271747..84294372hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3822626
hg1922626
hg1822626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573517
Supporting Variants
Samples
Known GenesGINS2, MIR7851
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv862306
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