A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064031



Internal ID18806562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:46202343..46298843hg38UCSC Ensembl
Innerchr18:43782309..43878806hg19UCSC Ensembl
Innerchr18:42036307..42132804hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3896501
hg1996498
hg1896498
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726072
Samples
Known GenesC18orf25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064031
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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