A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064386



Internal ID19153605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59985517..60002864hg38UCSC Ensembl
Innerchr18:57652749..57670096hg19UCSC Ensembl
Innerchr18:55803729..55821076hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3817348
hg1917348
hg1817348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3367n100
Supporting Variantsnssv3565539, nssv3565538
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)nsv1064386
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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