A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551534



Internal ID20924668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50089701..50090300hg38UCSC Ensembl
chr22:50528130..50528729hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074814
Samples
Known GenesMOV10L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551534
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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