A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023125



Internal ID19112342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153308618..153350848hg38UCSC Ensembl
Innerchr5:152688178..152730408hg19UCSC Ensembl
Innerchr5:152668371..152710601hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3842231
hg1942231
hg1842231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648187, nssv3746655
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)nsv1023125
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer