A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv986702



Internal ID16280658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195065244..195066625hg38UCSC Ensembl
Innerchr3:194785973..194787354hg19UCSC Ensembl
Innerchr3:196267262..196268643hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381382
hg191382
hg181382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592970
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)nssv986702
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