A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525577



Internal ID18823858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109631121..109710607hg38UCSC Ensembl
Innerchr13:110283468..110362954hg19UCSC Ensembl
Innerchr13:109081469..109160955hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3879487
hg1979487
hg1879487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051686
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)nssv3525577
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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