A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053206



Internal ID19142425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89812266..89868855hg38UCSC Ensembl
Innerchr13:90464520..90521109hg19UCSC Ensembl
Innerchr13:89262521..89319110hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3856590
hg1956590
hg1856590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713268
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)nsv1053206
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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