A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026958



Internal ID19116176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:86446094..86496130hg38UCSC Ensembl
Innerchr5:85741911..85791947hg19UCSC Ensembl
Innerchr5:85777667..85827703hg18UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3850037
hg1950037
hg1850037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639183
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)nsv1026958
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