A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695233



Internal ID15085199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7056359..7076731hg38UCSC Ensembl
Innerchr16:7106360..7126732hg19UCSC Ensembl
Innerchr16:7046361..7066733hg18UCSC Ensembl
Innerchr16:7046361..7066733hg17UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3820373
hg1920373
hg1820373
hg1720373
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517828
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695233
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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