A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3592277



Internal ID18890558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47998117..48038895hg38UCSC Ensembl
Innerchr22:48393866..48434712hg19UCSC Ensembl
Innerchr22:46772530..46813376hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3840779
hg1940847
hg1840847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063416
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3592277
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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