A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571398



Internal ID16358807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7726122..7753015hg38UCSC Ensembl
Innerchr16:7776124..7803017hg19UCSC Ensembl
Innerchr16:7716125..7743018hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3826894
hg1926894
hg1826894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150512
Samples1780854096_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571398
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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