A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063978



Internal ID19153197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071214..14233523hg38UCSC Ensembl
Innerchr18:14071213..14233522hg19UCSC Ensembl
Innerchr18:14061213..14223522hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38162310
hg19162310
hg18162310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3322n100
Supporting Variantsnssv3564113
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)nsv1063978
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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