A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055996



Internal ID19145215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071214..14285018hg38UCSC Ensembl
Innerchr18:14071213..14285017hg19UCSC Ensembl
Innerchr18:14061213..14275017hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38213805
hg19213805
hg18213805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3321n100
Supporting Variantsnssv3564116
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)nsv1055996
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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