A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169952



Internal ID21314013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:40335373..40351444hg38UCSC Ensembl
Outerchr5:40333830..40357561hg38UCSC Ensembl
Innerchr5:40335475..40351546hg19UCSC Ensembl
Outerchr5:40333932..40357663hg19UCSC Ensembl
Innerchr5:40371232..40387303hg18UCSC Ensembl
Outerchr5:40369689..40393420hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3823732
hg1923732
hg1823732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249785, nssv14241702
SamplesNGO_25, NGO_55
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169952
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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