A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063794



Internal ID19153013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071214..14227776hg38UCSC Ensembl
Innerchr18:14071213..14227775hg19UCSC Ensembl
Innerchr18:14061213..14217775hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38156563
hg19156563
hg18156563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3322n100
Supporting Variantsnssv3564112
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)nsv1063794
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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