A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515584



Internal ID15443195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:22465793..22486192hg38UCSC Ensembl
Innerchr18:20045756..20066155hg19UCSC Ensembl
Innerchr18:18299754..18320153hg18UCSC Ensembl
Innerchr18:18299754..18320153hg17UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3820400
hg1920400
hg1820400
hg1720400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665357, nssv657367, nssv664031, nssv678618, nssv680484, nssv682907, nssv669241, nssv685691, nssv664003, nssv678645, nssv674022, nssv659533, nssv690400, nssv656281, nssv659985, nssv665169, nssv679995, nssv679404, nssv673535, nssv668202
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515584
Frequency
Sample Size2026
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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