A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588946



Internal ID16376355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:34665571..34775640hg38UCSC Ensembl
Innerchr22:35061563..35171631hg19UCSC Ensembl
Innerchr22:33391563..33501631hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38110070
hg19110069
hg18110069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954752
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588946
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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