A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026614



Internal ID19115832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:146309058..146353653hg38UCSC Ensembl
Innerchr5:145688621..145733216hg19UCSC Ensembl
Innerchr5:145668814..145713409hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3844596
hg1944596
hg1844596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648159
Samples
Known GenesPOU4F3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026614
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