A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701461



Internal ID15091427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38864027..38885631hg38UCSC Ensembl
Innerchr22:39260032..39281636hg19UCSC Ensembl
Innerchr22:37589978..37611582hg18UCSC Ensembl
Innerchr22:37584532..37606136hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3821605
hg1921605
hg1821605
hg1721605
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525343
Supporting Variants
Samples
Known GenesCBX6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701461
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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