A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594850



Internal ID18893131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65202778..65230662hg38UCSC Ensembl
Innerchr3:65188453..65216337hg19UCSC Ensembl
Innerchr3:65163493..65191377hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3827885
hg1927885
hg1827885
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013444
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3594850
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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