A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014733



Internal ID19103950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:102253039..102285083hg38UCSC Ensembl
Innerchr4:103174196..103206240hg19UCSC Ensembl
Innerchr4:103393219..103425263hg18UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3832045
hg1932045
hg1832045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5348n100
Supporting Variantsnssv3631022
Samples
Known GenesSLC39A8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014733
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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