A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519407



Internal ID15100014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6695598..6696371hg38UCSC Ensembl
Innerchr16:6745599..6746372hg19UCSC Ensembl
Innerchr16:6685600..6686373hg18UCSC Ensembl
Innerchr16:6685600..6686373hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38774
hg19774
hg18774
hg17774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677299, nssv656005
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519407
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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