A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516355



Internal ID15443648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8734997..8735547hg38UCSC Ensembl
Innerchr18:8734995..8735545hg19UCSC Ensembl
Innerchr18:8724995..8725545hg18UCSC Ensembl
Innerchr18:8724995..8725545hg17UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38551
hg19551
hg18551
hg17551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667750, nssv673204
Samples
Known GenesSOGA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516355
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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