A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066089



Internal ID18808620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3923759..3964699hg38UCSC Ensembl
Innerchr18:3923759..3964699hg19UCSC Ensembl
Innerchr18:3913759..3954699hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3840941
hg1940941
hg1840941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725271
Samples
Known GenesDLGAP1, DLGAP1-AS4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066089
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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