A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701145



Internal ID15091111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113740525..114390328hg38UCSC Ensembl
Innerchr4:114661681..115311484hg19UCSC Ensembl
Innerchr4:114881130..115530933hg18UCSC Ensembl
Innerchr4:115019285..115669088hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38649804
hg19649804
hg18649804
hg17649804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525087
Supporting Variants
Samples
Known GenesARSJ, CAMK2D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701145
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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