A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592971



Internal ID16380380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195065244..195066739hg38UCSC Ensembl
Innerchr3:194785973..194787468hg19UCSC Ensembl
Innerchr3:196267262..196268757hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381496
hg191496
hg181496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8824n54
Supporting Variantsnssv986703
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592971
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