A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552604



Internal ID20925729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33139501..33216100hg38UCSC Ensembl
chr22:33535487..33612086hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3876600
hg1976600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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