A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597873



Internal ID20970944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27937956..27938363hg38UCSC Ensembl
chr22:28333944..28334351hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254845
Samples
Known GenesTTC28-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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