A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599037



Internal ID20972108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29100327..29101013hg38UCSC Ensembl
chr22:29496315..29497001hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255486
Samples
Known GenesKREMEN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599037
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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