A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517425



Internal ID15444718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:47457010..47471653hg38UCSC Ensembl
Innerchr18:44983381..44998024hg19UCSC Ensembl
Innerchr18:43237379..43252022hg18UCSC Ensembl
Innerchr18:43237379..43252022hg17UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3814644
hg1914644
hg1814644
hg1714644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694123, nssv651982, nssv653139
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517425
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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