A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554505



Internal ID20927599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32846452..32847258hg38UCSC Ensembl
chr22:33242439..33243245hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073800
Samples
Known GenesSYN3, TIMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554505
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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