A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051678



Internal ID19140897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101406036..101608463hg38UCSC Ensembl
Innerchr15:101946241..102148666hg19UCSC Ensembl
Innerchr15:99763764..99966189hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38202428
hg19202426
hg18202426
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2676n100
Supporting Variantsnssv3555345
Samples
Known GenesPCSK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051678
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