A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170040



Internal ID21314101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25410259..25480195hg38UCSC Ensembl
Outerchr5:25405958..25485709hg38UCSC Ensembl
Innerchr5:25410368..25480304hg19UCSC Ensembl
Outerchr5:25406067..25485818hg19UCSC Ensembl
Innerchr5:25446125..25516061hg18UCSC Ensembl
Outerchr5:25441824..25521575hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3879752
hg1979752
hg1879752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247379, nssv14252460
SamplesNGO_32, NGO_24
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170040
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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