A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014675



Internal ID18757210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:2966495..3010996hg38UCSC Ensembl
Innerchr4:2968222..3012723hg19UCSC Ensembl
Innerchr4:2938020..2982521hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3844502
hg1944502
hg1844502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5082n100
Supporting Variantsnssv3616113
Samples
Known GenesGRK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014675
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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