A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744558



Internal ID18696153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189847201..189961635hg38UCSC Ensembl
Innerchr4:190768356..190882790hg19UCSC Ensembl
Innerchr4:191005350..191119784hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38114435
hg19114435
hg18114435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017070
Supporting Variants
Samples
Known GenesFRG1, LOC283788
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3744558
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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