A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700460



Internal ID15090426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113918114..114701151hg38UCSC Ensembl
Innerchr4:114839270..115622307hg19UCSC Ensembl
Innerchr4:115058719..115841756hg18UCSC Ensembl
Innerchr4:115196874..115979911hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38783038
hg19783038
hg18783038
hg17783038
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524515
Supporting Variants
Samples
Known GenesARSJ, MIR577, UGT8
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700460
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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