A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954752



Internal ID16248708
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 StatusS
Merged Variantsnsv588946
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv954752
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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