A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543438



Internal ID20916686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197531922..197532618hg38UCSC Ensembl
chr2:198396646..198397342hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257113
Samples
Known GenesHSPE1-MOB4, MOB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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