A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515746



Internal ID15096353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85591521..85651514hg38UCSC Ensembl
Innerchr16:85625127..85685120hg19UCSC Ensembl
Innerchr16:84182628..84242621hg18UCSC Ensembl
Innerchr16:84182628..84242621hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3859994
hg1959994
hg1859994
hg1759994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684299, nssv664653
Samples
Known GenesGSE1, MIR7851
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515746
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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