A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528746



Internal ID15109353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6898632..6982052hg38UCSC Ensembl
Innerchr16:6948633..7032053hg19UCSC Ensembl
Innerchr16:6888634..6972054hg18UCSC Ensembl
Innerchr16:6888634..6972054hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3883421
hg1983421
hg1883421
hg1783421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705407
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528746
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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