A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055209



Internal ID18797740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37368942..37407677hg38UCSC Ensembl
Innerchr18:34948905..34987640hg19UCSC Ensembl
Innerchr18:33202903..33241638hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3838736
hg1938736
hg1838736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3336n100
Supporting Variantsnssv3564207
Samples
Known GenesCELF4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055209
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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