A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv962142



Internal ID16256098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35965622..36058573hg38UCSC Ensembl
Innerchr3:36007114..36100065hg19UCSC Ensembl
Innerchr3:35982118..36075069hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3892952
hg1992952
hg1892952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv962142
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