A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061346



Internal ID19150565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59981043..60002864hg38UCSC Ensembl
Innerchr18:57648275..57670096hg19UCSC Ensembl
Innerchr18:55799255..55821076hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3821822
hg1921822
hg1821822
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3367n100
Supporting Variantsnssv3565500
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)nsv1061346
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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