A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026854



Internal ID18769385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168979569..169055953hg38UCSC Ensembl
Innerchr4:169900720..169977104hg19UCSC Ensembl
Innerchr4:170137295..170213679hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3876385
hg1976385
hg1876385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3744509
Samples
Known GenesCBR4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026854
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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