A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039333



Internal ID19128552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:79715801..79759032hg38UCSC Ensembl
Innerchr13:80289936..80333167hg19UCSC Ensembl
Innerchr13:79187937..79231168hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3843232
hg1943232
hg1843232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530519
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)nsv1039333
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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