A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169519



Internal ID21313752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116487878..116496892hg38UCSC Ensembl
Outerchr3:116485454..116498768hg38UCSC Ensembl
Innerchr3:116206725..116215739hg19UCSC Ensembl
Outerchr3:116204301..116217615hg19UCSC Ensembl
Innerchr3:117689415..117698429hg18UCSC Ensembl
Outerchr3:117686991..117700305hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3813315
hg1913315
hg1813315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247038
SamplesNGO_53
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169519
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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