A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597187



Internal ID20970258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29001475..29003529hg38UCSC Ensembl
chr22:29397463..29399517hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255484
Samples
Known GenesZNRF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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