A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564069



Internal ID18515664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3494893..3572306hg38UCSC Ensembl
Innerchr18:3494891..3572304hg19UCSC Ensembl
Innerchr18:3484891..3562304hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3877414
hg1977414
hg1877414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059696
Supporting Variants
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564069
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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