A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169964



Internal ID21314025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84217648..84267664hg38UCSC Ensembl
Outerchr3:84214513..84278110hg38UCSC Ensembl
Innerchr3:84266799..84316815hg19UCSC Ensembl
Outerchr3:84263664..84327261hg19UCSC Ensembl
Innerchr3:84349489..84399505hg18UCSC Ensembl
Outerchr3:84346354..84409951hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3863598
hg1963598
hg1863598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248980, nssv14252012
SamplesNGO_12, NGO_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169964
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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