A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046079



Internal ID18788610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101304719..101370019hg38UCSC Ensembl
Innerchr15:101844924..101910224hg19UCSC Ensembl
Innerchr15:99662447..99727747hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3865301
hg1965301
hg1865301
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555337
Samples
Known GenesLOC100507472, PCSK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046079
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