A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060354



Internal ID19149573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:67896823..67985900hg38UCSC Ensembl
Innerchr18:65564060..65653137hg19UCSC Ensembl
Innerchr18:63715040..63804117hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3889078
hg1989078
hg1889078
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3388n100
Supporting Variantsnssv3566447
Samples
Known GenesLOC643542
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060354
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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