A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3744565



Internal ID19042846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:189903701..189988277hg38UCSC Ensembl
Innerchr4:190824856..190909432hg19UCSC Ensembl
Innerchr4:191061850..191146426hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3884577
hg1984577
hg1884577
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034108
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)nssv3744565
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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