A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059986



Internal ID19149205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24274010..24413936hg38UCSC Ensembl
Innerchr19:24456812..24596738hg19UCSC Ensembl
Innerchr19:24248652..24388578hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38139927
hg19139927
hg18139927
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3489n100
Supporting Variantsnssv3570717, nssv3570718
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)nsv1059986
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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