A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055437



Internal ID19144656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59687325..59705236hg38UCSC Ensembl
Innerchr18:57354557..57372468hg19UCSC Ensembl
Innerchr18:55505537..55523448hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3817912
hg1917912
hg1817912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565499
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)nsv1055437
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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