A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210985



Internal ID22358694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24605966..24606034hg38UCSC Ensembl
chr22:25001933..25002001hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5697n152
Supporting Variantsnssv14304054, nssv14304053, nssv14304055
SamplesHG00512, HG00732, HG00514
Known GenesGGT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210985
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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