A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703348



Internal ID15093314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:150754667..151133921hg38UCSC Ensembl
Innerchr4:151675819..152055073hg19UCSC Ensembl
Innerchr4:151895269..152274523hg18UCSC Ensembl
Innerchr4:152033424..152412678hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38379255
hg19379255
hg18379255
hg17379255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526976
Supporting Variants
Samples
Known GenesLRBA, RPS3A, SH3D19, SNORD73A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703348
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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