A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251565



Internal ID21303062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65267773..65275718hg38UCSC Ensembl
Outerchr14:65263803..65282412hg38UCSC Ensembl
Innerchr14:65734491..65742436hg19UCSC Ensembl
Outerchr14:65730521..65749130hg19UCSC Ensembl
Innerchr14:64804244..64812189hg18UCSC Ensembl
Outerchr14:64800274..64818883hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3818610
hg1918610
hg1818610
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169495
Supporting Variants
SamplesMLY_3
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251565
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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