A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037402



Internal ID19126621
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 StatusM
Merged Variantsdgv1714n100
Supporting Variantsnssv3529387
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)nsv1037402
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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