A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543269



Internal ID20916521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223754767..223755606hg38UCSC Ensembl
chr2:224619484..224620323hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257124
Samples
Known GenesAP1S3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543269
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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