A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3614979



Internal ID18913260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177488087..177513527hg38UCSC Ensembl
Innerchr3:177205875..177231315hg19UCSC Ensembl
Innerchr3:178688569..178714009hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3825441
hg1925441
hg1825441
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014893
Supporting Variants
Samples
Known GenesLINC00578
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3614979
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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