A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059428



Internal ID18801959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:842299..987971hg38UCSC Ensembl
Innerchr17:745539..891211hg19UCSC Ensembl
Innerchr17:692289..837961hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38145673
hg19145673
hg18145673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3078n100
Supporting Variantsnssv3560057
Samples
Known GenesNXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059428
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