A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592973



Internal ID16380382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195065347..195066565hg38UCSC Ensembl
Innerchr3:194786076..194787294hg19UCSC Ensembl
Innerchr3:196267365..196268583hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381219
hg191219
hg181219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8824n54
Supporting Variantsnssv986705
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592973
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