A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522167



Internal ID15102774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7138252..7151444hg38UCSC Ensembl
Innerchr16:7188253..7201445hg19UCSC Ensembl
Innerchr16:7128254..7141446hg18UCSC Ensembl
Innerchr16:7128254..7141446hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3813193
hg1913193
hg1813193
hg1713193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694940
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522167
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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