A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026511



Internal ID18769043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:151672230..151690763hg38UCSC Ensembl
Innerchr4:152593382..152611915hg19UCSC Ensembl
Innerchr4:152812832..152831365hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3818534
hg1918534
hg1818534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3636093
Samples
Known GenesPET112
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026511
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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