A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111204



Internal ID22020437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:24605932..24605932hg38UCSC Ensembl
chr22:25001899..25001899hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641467
Samples
Known GenesGGT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111204
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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