A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063019



Internal ID19152238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071214..14262531hg38UCSC Ensembl
Innerchr18:14071213..14262530hg19UCSC Ensembl
Innerchr18:14061213..14252530hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38191318
hg19191318
hg18191318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3321n100
Supporting Variantsnssv3564115, nssv3564114
Samples
Known GenesANKRD20A5P, ZNF519
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063019
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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