A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066095



Internal ID18808626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4845604..5263909hg38UCSC Ensembl
Innerchr18:4845603..5263908hg19UCSC Ensembl
Innerchr18:4835603..5253908hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38418306
hg19418306
hg18418306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564079
Samples
Known GenesC18orf42, LINC00526, LINC00667
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066095
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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