A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064666



Internal ID19153885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:43857645..43901624hg38UCSC Ensembl
Innerchr18:41437610..41481589hg19UCSC Ensembl
Innerchr18:39691608..39735587hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3843980
hg1943980
hg1843980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565368
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064666
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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