A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv363n21



Internal ID18990836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176931607..177242486hg38UCSC Ensembl
chr5:176358608..176669487hg19UCSC Ensembl
chr5:176291214..176602093hg18UCSC Ensembl
chr5:176291214..176602093hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38310880
hg19310880
hg18310880
hg17310880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523163, nsv524656
Samples
Known GenesFGFR4, NSD1, UIMC1, ZNF346
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv363n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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