A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529387



Internal ID18827668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70285697..70309696hg38UCSC Ensembl
Innerchr13:70859829..70883828hg19UCSC Ensembl
Innerchr13:69757830..69781829hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3824000
hg1924000
hg1824000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037402
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)nssv3529387
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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