A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744559



Internal ID18696154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189870388..190052393hg38UCSC Ensembl
Innerchr4:190791543..190973548hg19UCSC Ensembl
Innerchr4:191028537..191210542hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38182006
hg19182006
hg18182006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029979
Supporting Variants
Samples
Known GenesFRG1, FRG2, LOC100288255, LOC283788
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3744559
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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