A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146884



Internal ID346090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:22196265..22899568hg38UCSC Ensembl
chr22:22550665..23241748hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38703304
hg19691084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv324n206
Supporting Variantsnssv17727857
Samples
Known GenesBMS1P20, GGTLC2, IGLL5, LOC648691, MIR650, POM121L1P, PRAME, VPREB1, ZNF280A, ZNF280B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6146884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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