A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229013



Internal ID22371001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37559350..37559466hg38UCSC Ensembl
chr22:37955357..37955473hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14303543, nssv14303544
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229013
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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