A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613017



Internal ID16400426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:515616..527438hg38UCSC Ensembl
Innerchr9:515616..527438hg19UCSC Ensembl
Innerchr9:505616..517438hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3811823
hg1911823
hg1811823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12454n54
Supporting Variantsnssv1125979
Samples
Known GenesKANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613017
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