A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020558



Internal ID19109777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:21688564..21748017hg38UCSC Ensembl
Innerchr5:21688673..21748126hg19UCSC Ensembl
Innerchr5:21724430..21783883hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3859454
hg1959454
hg1859454
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745849
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)nsv1020558
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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