A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055343



Internal ID19144562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12107013..12226357hg38UCSC Ensembl
Innerchr18:12107012..12226356hg19UCSC Ensembl
Innerchr18:12097012..12216356hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38119345
hg19119345
hg18119345
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564106
Samples
Known GenesANKRD62, C18orf61
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055343
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer