A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024919



Internal ID19114136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186349230..186378545hg38UCSC Ensembl
Innerchr4:187270384..187299699hg19UCSC Ensembl
Innerchr4:187507378..187536693hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3829316
hg1929316
hg1829316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635635
Samples
Known GenesF11-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024919
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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