A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169799



Internal ID21313610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:236143357..236145113hg38UCSC Ensembl
Outerchr2:236140207..236154321hg38UCSC Ensembl
Innerchr2:237052001..237053757hg19UCSC Ensembl
Outerchr2:237048851..237062965hg19UCSC Ensembl
Innerchr2:236716740..236718496hg18UCSC Ensembl
Outerchr2:236713590..236727704hg18UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3814115
hg1914115
hg1814115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244615
SamplesMLY_12
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169799
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer