A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015895



Internal ID19105113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17630..157741hg38UCSC Ensembl
Innerchr5:17630..157856hg19UCSC Ensembl
Innerchr5:70630..210856hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38140112
hg19140227
hg18140227
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5515n100
Supporting Variantsnssv3633200
Samples
Known GenesPLEKHG4B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015895
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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