A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613016



Internal ID16400425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:515616..526772hg38UCSC Ensembl
Innerchr9:515616..526772hg19UCSC Ensembl
Innerchr9:505616..516772hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3811157
hg1911157
hg1811157
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12454n54
Supporting Variantsnssv1156407, nssv1156405, nssv1156406
SamplesHGDP01202, HGDP00460, HGDP00458
Known GenesKANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613016
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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