A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061759



Internal ID19150978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71398505..71430311hg38UCSC Ensembl
Innerchr18:69065741..69097547hg19UCSC Ensembl
Innerchr18:67216721..67248527hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3831807
hg1931807
hg1831807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562969
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)nsv1061759
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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