A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14252460



Internal ID21307183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25410259..25463587hg38UCSC Ensembl
Outerchr5:25405958..25470404hg38UCSC Ensembl
Innerchr5:25410368..25463696hg19UCSC Ensembl
Outerchr5:25406067..25470513hg19UCSC Ensembl
Innerchr5:25446125..25499453hg18UCSC Ensembl
Outerchr5:25441824..25506270hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3864447
hg1964447
hg1864447
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170040
Supporting Variants
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14252460
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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