A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528898



Internal ID15109505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88805821..88827008hg38UCSC Ensembl
Innerchr16:88872229..88893416hg19UCSC Ensembl
Innerchr16:87399730..87420917hg18UCSC Ensembl
Innerchr16:87399730..87420917hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3821188
hg1921188
hg1821188
hg1721188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705582
Samples
Known GenesAPRT, CDT1, GALNS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528898
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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