A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242603



Internal ID21306200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:142202639..142207042hg38UCSC Ensembl
Outerchr5:142200306..142214063hg38UCSC Ensembl
Innerchr5:141582204..141586607hg19UCSC Ensembl
Outerchr5:141579871..141593628hg19UCSC Ensembl
Innerchr5:141562388..141566791hg18UCSC Ensembl
Outerchr5:141560055..141573812hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3813758
hg1913758
hg1813758
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170237
Supporting Variants
SamplesNGO_26
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242603
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