A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518140



Internal ID15098747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32240814..32257740hg38UCSC Ensembl
Innerchr8:32098330..32115256hg19UCSC Ensembl
Innerchr8:32217872..32234798hg18UCSC Ensembl
Innerchr8:32217872..32234798hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3816927
hg1916927
hg1816927
hg1716927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695561
Samples
Known GenesNRG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518140
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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