A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039012



Internal ID18781543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:40217600..40369658hg38UCSC Ensembl
Innerchr13:40791737..40943795hg19UCSC Ensembl
Innerchr13:39689737..39841795hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38152059
hg19152059
hg18152059
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1633n100
Supporting Variantsnssv3523390
Samples
Known GenesLINC00548, LINC00598
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039012
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer