A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516152



Internal ID15096759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4322214..4335455hg38UCSC Ensembl
Innerchr18:4322214..4335455hg19UCSC Ensembl
Innerchr18:4312214..4325455hg18UCSC Ensembl
Innerchr18:4312214..4325455hg17UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3813242
hg1913242
hg1813242
hg1713242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv686641, nssv682490, nssv690154, nssv674506, nssv678050, nssv693693, nssv673477, nssv674830, nssv705961, nssv665122, nssv665993, nssv683590, nssv658068, nssv678845, nssv678005, nssv670650, nssv659268, nssv684930, nssv652553, nssv680346
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516152
Frequency
Sample Size2026
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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