A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047026



Internal ID19136245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109615907..109654407hg38UCSC Ensembl
Innerchr13:110268254..110306754hg19UCSC Ensembl
Innerchr13:109066255..109104755hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3838501
hg1938501
hg1838501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713305
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)nsv1047026
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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