A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247964



Internal ID21301647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:125724765..125739919hg38UCSC Ensembl
Outerchr3:125717394..125743486hg38UCSC Ensembl
Innerchr3:125443608..125458762hg19UCSC Ensembl
Outerchr3:125436237..125462329hg19UCSC Ensembl
Innerchr3:126926298..126941452hg18UCSC Ensembl
Outerchr3:126918927..126945019hg18UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3826093
hg1926093
hg1826093
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170005
Supporting Variants
SamplesMLY_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247964
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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