A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059793



Internal ID19149012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:35259520..35361982hg38UCSC Ensembl
Innerchr18:32839484..32941946hg19UCSC Ensembl
Innerchr18:31093482..31195944hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38102463
hg19102463
hg18102463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564195
Samples
Known GenesZNF24, ZNF271, ZSCAN30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059793
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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