A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169694



Internal ID21313505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:81158615..81172052hg38UCSC Ensembl
Outerchr5:81151807..81175302hg38UCSC Ensembl
Innerchr5:80454434..80467871hg19UCSC Ensembl
Outerchr5:80447626..80471121hg19UCSC Ensembl
Innerchr5:80490190..80503627hg18UCSC Ensembl
Outerchr5:80483382..80506877hg18UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3823496
hg1923496
hg1823496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245736
SamplesMLY_14
Known GenesRASGRF2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169694
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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