A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696483



Internal ID15086449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38172999..38210773hg38UCSC Ensembl
Innerchr22:38569006..38606780hg19UCSC Ensembl
Innerchr22:36898952..36936726hg18UCSC Ensembl
Innerchr22:36893506..36931280hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3837775
hg1937775
hg1837775
hg1737775
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519015
Supporting Variants
Samples
Known GenesMAFF, PLA2G6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696483
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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