A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554879



Internal ID20927969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41848087..41859931hg38UCSC Ensembl
chr22:42244091..42255935hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3811845
hg1911845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074542
Samples
Known GenesSREBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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