A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17727584



Internal ID151250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18767000..18795564hg38UCSC Ensembl
chr22:18754513..18783077hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3828565
hg1928565
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146640
Supporting Variants
Samples
Known GenesGGT3P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17727584
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.123371


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