A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060736



Internal ID19149955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78421827..78551855hg38UCSC Ensembl
Innerchr18:76181827..76311855hg19UCSC Ensembl
Innerchr18:74282815..74412843hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38130029
hg19130029
hg18130029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563047
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060736
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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