A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3488865



Internal ID18729820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:180158481..180222116hg38UCSC Ensembl
Innerchr1:180127616..180191251hg19UCSC Ensembl
Innerchr1:178394239..178457874hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3863636
hg1963636
hg1863636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000954
Supporting Variants
Samples
Known GenesFLJ23867, QSOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3488865
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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