A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063759



Internal ID19152978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:31973728..32003781hg38UCSC Ensembl
Innerchr18:29553691..29583744hg19UCSC Ensembl
Innerchr18:27807689..27837742hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3830054
hg1930054
hg1830054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3329n100
Supporting Variantsnssv3564167
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)nsv1063759
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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