A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024281



Internal ID19113498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:53966507..53986505hg38UCSC Ensembl
Innerchr5:53262337..53282335hg19UCSC Ensembl
Innerchr5:53298094..53318092hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3819999
hg1919999
hg1819999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642133
Samples
Known GenesARL15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024281
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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