A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059812



Internal ID19149031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:15093592..15401752hg38UCSC Ensembl
Innerchr18:15093591..15401751hg19UCSC Ensembl
Innerchr18:15083591..15391751hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg38308161
hg19308161
hg18308161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3323n100
Supporting Variantsnssv3725295
Samples
Known GenesLOC644669
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059812
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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