A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013936



Internal ID18756468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:67375363..67472988hg38UCSC Ensembl
Innerchr4:68241081..68338706hg19UCSC Ensembl
Innerchr4:67923676..68021301hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3897626
hg1997626
hg1897626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5241n100
Supporting Variantsnssv3626806
Samples
Known GenesCENPC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013936
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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