A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066881



Internal ID18809412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31569789..31600877hg38UCSC Ensembl
Innerchr18:29149752..29180840hg19UCSC Ensembl
Innerchr18:27403750..27434838hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3831089
hg1931089
hg1831089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725310
Samples
Known GenesTTR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066881
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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