A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057526



Internal ID19146745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59685542..59741462hg38UCSC Ensembl
Innerchr18:57352774..57408694hg19UCSC Ensembl
Innerchr18:55503754..55559674hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3855921
hg1955921
hg1855921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3366n100
Supporting Variantsnssv3565498
Samples
Known GenesCCBE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057526
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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