A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176470



Internal ID15529335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114154651..114178138hg38UCSC Ensembl
Innerchr9:116916931..116940418hg19UCSC Ensembl
Innerchr9:115956752..115980239hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3823488
hg1923488
hg1823488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615231
Supporting Variants
SamplesHGDP00774
Known GenesCOL27A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176470
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