A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057972



Internal ID19147191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59984977..59995464hg38UCSC Ensembl
Innerchr18:57652209..57662696hg19UCSC Ensembl
Innerchr18:55803189..55813676hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3810488
hg1910488
hg1810488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3368n100
Supporting Variantsnssv3565502
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)nsv1057972
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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