A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535924



Internal ID20909277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30182422..30198704hg38UCSC Ensembl
chr22:30578411..30594693hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3816283
hg1916283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535924
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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