A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058379



Internal ID19147598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:48840217..48855578hg38UCSC Ensembl
Innerchr18:46366588..46381949hg19UCSC Ensembl
Innerchr18:44620586..44635947hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3815362
hg1915362
hg1815362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565438
Samples
Known GenesCTIF
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058379
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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