A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696555



Internal ID15433207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:49814973..49847562hg38UCSC Ensembl
Innerchr22:50208621..50241210hg19UCSC Ensembl
Innerchr22:48594625..48627214hg18UCSC Ensembl
Innerchr22:48529482..48562071hg17UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3832590
hg1932590
hg1832590
hg1732590
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519083
Supporting Variants
Samples
Known GenesBRD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696555
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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