A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020578



Internal ID19109797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:106546117..106597258hg38UCSC Ensembl
Innerchr5:105881818..105932959hg19UCSC Ensembl
Innerchr5:105909717..105960858hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3851142
hg1951142
hg1851142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3646935
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)nsv1020578
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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