A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551234



Internal ID20924371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42923498..42934932hg38UCSC Ensembl
chr22:43319504..43330938hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3811435
hg1911435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074360
Samples
Known GenesPACSIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551234
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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