A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521752



Internal ID15449045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:50839084..50840844hg38UCSC Ensembl
Innerchr16:50872995..50874755hg19UCSC Ensembl
Innerchr16:49430496..49432256hg18UCSC Ensembl
Innerchr16:49430496..49432256hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381761
hg191761
hg181761
hg171761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694094
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521752
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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