A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019123



Internal ID19108341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15520..161267hg38UCSC Ensembl
Innerchr5:15520..161382hg19UCSC Ensembl
Innerchr5:68520..214382hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38145748
hg19145863
hg18145863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5515n100
Supporting Variantsnssv3636536
Samples
Known GenesPLEKHG4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019123
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