A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248980



Internal ID21304532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84217648..84260361hg38UCSC Ensembl
Outerchr3:84214513..84265246hg38UCSC Ensembl
Innerchr3:84266799..84309512hg19UCSC Ensembl
Outerchr3:84263664..84314397hg19UCSC Ensembl
Innerchr3:84349489..84392202hg18UCSC Ensembl
Outerchr3:84346354..84397087hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3850734
hg1950734
hg1850734
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169964
Supporting Variants
SamplesNGO_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248980
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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