A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216122



Internal ID22362227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45929870..45929948hg38UCSC Ensembl
chr22:46325750..46325828hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305147
SamplesHG00514
Known GenesWNT7B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216122
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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