A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047134



Internal ID19136353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86441993..86704674hg38UCSC Ensembl
Innerchr13:87094248..87356929hg19UCSC Ensembl
Innerchr13:85892249..86154930hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38262682
hg19262682
hg18262682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713256
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)nsv1047134
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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