A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250286



Internal ID21303345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65267773..65285606hg38UCSC Ensembl
Outerchr14:65263803..65291030hg38UCSC Ensembl
Innerchr14:65734491..65752324hg19UCSC Ensembl
Outerchr14:65730521..65757748hg19UCSC Ensembl
Innerchr14:64804244..64822077hg18UCSC Ensembl
Outerchr14:64800274..64827501hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3827228
hg1927228
hg1827228
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169495
Supporting Variants
SamplesMLY_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250286
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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