A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016811



Internal ID19106028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:29786825..29824489hg38UCSC Ensembl
Innerchr5:29786932..29824596hg19UCSC Ensembl
Innerchr5:29822689..29860353hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3837665
hg1937665
hg1837665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5615n100
Supporting Variantsnssv3636022
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016811
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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