A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063095



Internal ID19152314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70439183..70639700hg38UCSC Ensembl
Innerchr17:68435324..68635841hg19UCSC Ensembl
Innerchr17:65946919..66147436hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38200518
hg19200518
hg18200518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3278n100
Supporting Variantsnssv3567762
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)nsv1063095
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