A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3616105



Internal ID18567700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1676066..1710725hg38UCSC Ensembl
Innerchr4:1677793..1712452hg19UCSC Ensembl
Innerchr4:1647591..1682250hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3834660
hg1934660
hg1834660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014440
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)nssv3616105
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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