A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599373



Internal ID20972444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29006001..29006410hg38UCSC Ensembl
chr22:29401989..29402398hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255485
Samples
Known GenesZNRF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599373
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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