A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036855



Internal ID19126074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103444213..103520940hg38UCSC Ensembl
Innerchr13:104096563..104173290hg19UCSC Ensembl
Innerchr13:102894564..102971291hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3876728
hg1976728
hg1876728
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1734n100
Supporting Variantsnssv3525545
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)nsv1036855
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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