A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14304055



Internal ID22203856
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3210985
Supporting Variants
SamplesHG00732
Known GenesGGT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14304055
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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