A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061832



Internal ID19151051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:40237274..40268564hg38UCSC Ensembl
Innerchr18:37817238..37848528hg19UCSC Ensembl
Innerchr18:36071236..36102526hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3831291
hg1931291
hg1831291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3339n100
Supporting Variantsnssv3564221, nssv3565329
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)nsv1061832
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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