A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169495



Internal ID21313978
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243434, nssv14241087, nssv14251565, nssv14250286, nssv14246458
SamplesMLY_5, MLY_17, MLY_3, SNI_6, SNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169495
Frequency
Sample Size93
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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