A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957090



Internal ID16251046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:41731777..41819680hg38UCSC Ensembl
Innerchr22:42127781..42215684hg19UCSC Ensembl
Innerchr22:40457727..40545630hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3887904
hg1987904
hg1887904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589052
Supporting Variants
Samples
Known GenesCCDC134, MEI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957090
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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