A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151123



Internal ID15878412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194382880..194501360hg38UCSC Ensembl
Innerchr2:195247604..195366084hg19UCSC Ensembl
Innerchr2:194955849..195074329hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38118481
hg19118481
hg18118481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584102
Supporting Variants
SamplesHGDP01197
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151123
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