A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043972



Internal ID18786503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68331033..68350422hg38UCSC Ensembl
Innerchr15:68623371..68642760hg19UCSC Ensembl
Innerchr15:66410425..66429814hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3819390
hg1919390
hg1819390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3553660
Samples
Known GenesITGA11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043972
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