A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704773



Internal ID15441425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66408417..66493179hg38UCSC Ensembl
Innerchr4:67274135..67358897hg19UCSC Ensembl
Innerchr4:66956730..67041492hg18UCSC Ensembl
Innerchr4:67102901..67187663hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3884763
hg1984763
hg1884763
hg1784763
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528212
Supporting Variants
Samples
Known GenesMIR548AJ2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704773
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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