A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061553



Internal ID19150772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:73749757..73828250hg38UCSC Ensembl
Innerchr18:71416992..71495485hg19UCSC Ensembl
Innerchr18:69567972..69646465hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3878494
hg1978494
hg1878494
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3563000
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)nsv1061553
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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