A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744265



Internal ID18695860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150743286..151146257hg38UCSC Ensembl
Innerchr4:151664438..152067409hg19UCSC Ensembl
Innerchr4:151883888..152286859hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38402972
hg19402972
hg18402972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018404
Supporting Variants
Samples
Known GenesLRBA, RPS3A, SH3D19, SNORD73A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3744265
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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