A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246963



Internal ID21307095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25156146..25302082hg38UCSC Ensembl
Outerchr5:25142982..25317541hg38UCSC Ensembl
Innerchr5:25156255..25302191hg19UCSC Ensembl
Outerchr5:25143091..25317650hg19UCSC Ensembl
Innerchr5:25192012..25337948hg18UCSC Ensembl
Outerchr5:25178848..25353407hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38174560
hg19174560
hg18174560
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170283
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)nssv14246963
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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