A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152211



Internal ID15874789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:50024802..50157413hg38UCSC Ensembl
Innerchr22:50463231..50595842hg19UCSC Ensembl
Innerchr22:48805358..48937969hg18UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38132612
hg19132612
hg18132612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589206
Supporting Variants
SamplesHGDP00590
Known GenesMLC1, MOV10L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152211
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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