A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010450



Internal ID19099667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77260884..77396686hg38UCSC Ensembl
Innerchr4:78182037..78317840hg19UCSC Ensembl
Innerchr4:78401061..78536864hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38135803
hg19135804
hg18135804
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5326n100
Supporting Variantsnssv3633866
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010450
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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