A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057441



Internal ID18799972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74344906..74669985hg38UCSC Ensembl
Innerchr18:72012141..72381941hg19UCSC Ensembl
Innerchr18:70163121..70510929hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38325080
hg19369801
hg18347809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3723230
Samples
Known GenesC18orf63, CNDP1, CNDP2, FAM69C, LINC00909, ZNF407
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057441
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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