A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616107



Internal ID18567702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1680529..1710725hg38UCSC Ensembl
Innerchr4:1682256..1712452hg19UCSC Ensembl
Innerchr4:1652054..1682250hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3830197
hg1930197
hg1830197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011292
Supporting Variants
Samples
Known GenesFAM53A, SLBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3616107
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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