A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065830



Internal ID18808361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:2263727..2576042hg38UCSC Ensembl
Innerchr18:2263727..2576041hg19UCSC Ensembl
Innerchr18:2253727..2566041hg18UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38312316
hg19312315
hg18312315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564059
Samples
Known GenesMETTL4, NDC80
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065830
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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