A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053354



Internal ID19142573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70285697..70312228hg38UCSC Ensembl
Innerchr13:70859829..70886360hg19UCSC Ensembl
Innerchr13:69757830..69784361hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3826532
hg1926532
hg1826532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1714n100
Supporting Variantsnssv3530495
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)nsv1053354
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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