A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703895



Internal ID15093861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35769058..35780530hg38UCSC Ensembl
Innerchr22:36165105..36176577hg19UCSC Ensembl
Innerchr22:34495051..34506523hg18UCSC Ensembl
Innerchr22:34489605..34501077hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3811473
hg1911473
hg1811473
hg1711473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527454
Supporting Variants
Samples
Known GenesRBFOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703895
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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