A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019409



Internal ID19108627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:108598327..108655725hg38UCSC Ensembl
Innerchr5:107934028..107991426hg19UCSC Ensembl
Innerchr5:107961927..108019325hg18UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3857399
hg1957399
hg1857399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3746556
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)nsv1019409
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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