A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016024



Internal ID19105242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120125101..120173362hg38UCSC Ensembl
Innerchr5:119460796..119509057hg19UCSC Ensembl
Innerchr5:119488695..119536956hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3848262
hg1948262
hg1848262
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5796n100
Supporting Variantsnssv3746600
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)nsv1016024
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