A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066939



Internal ID19156158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:38373037..38439188hg38UCSC Ensembl
Innerchr18:35953001..36019152hg19UCSC Ensembl
Innerchr18:34206999..34273150hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3866152
hg1966152
hg1866152
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564213
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)nsv1066939
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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