A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553934



Internal ID20927044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37018501..37024800hg38UCSC Ensembl
chr22:37414542..37420841hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074894
Samples
Known GenesMPST, TST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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