A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019391



Internal ID18761925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31200455..31464868hg38UCSC Ensembl
Innerchr5:31200562..31464975hg19UCSC Ensembl
Innerchr5:31236319..31500732hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38264414
hg19264414
hg18264414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5619n100
Supporting Variantsnssv3636029
Samples
Known GenesCDH6, DROSHA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019391
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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