A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525047



Internal ID15105654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7059008..7061526hg38UCSC Ensembl
Innerchr16:7109009..7111527hg19UCSC Ensembl
Innerchr16:7049010..7051528hg18UCSC Ensembl
Innerchr16:7049010..7051528hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg382519
hg192519
hg182519
hg172519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701092
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525047
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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