A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047759



Internal ID19136978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85294816..85329115hg38UCSC Ensembl
Innerchr13:85868951..85903250hg19UCSC Ensembl
Innerchr13:84766952..84801251hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3834300
hg1934300
hg1834300
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525415
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)nsv1047759
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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