A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169606



Internal ID21313839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:115370746..115385384hg38UCSC Ensembl
Outerchr5:115369510..115387269hg38UCSC Ensembl
Innerchr5:114706443..114721081hg19UCSC Ensembl
Outerchr5:114705207..114722966hg19UCSC Ensembl
Innerchr5:114734342..114748980hg18UCSC Ensembl
Outerchr5:114733106..114750865hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3817760
hg1917760
hg1817760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249260, nssv14241443, nssv14244188
SamplesNGO_3, MLY_9, PML_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169606
Frequency
Sample Size93
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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