A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063590



Internal ID18806121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4251031..4311534hg38UCSC Ensembl
Innerchr18:4251031..4311534hg19UCSC Ensembl
Innerchr18:4241031..4301534hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3860504
hg1960504
hg1860504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3315n100
Supporting Variantsnssv3564071
Samples
Known GenesDLGAP1, DLGAP1-AS5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063590
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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