A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040676



Internal ID19129895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63204173..63263121hg38UCSC Ensembl
Innerchr13:63778306..63837254hg19UCSC Ensembl
Innerchr13:62676307..62735255hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3858949
hg1958949
hg1858949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3526603
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)nsv1040676
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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