A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542484



Internal ID20915743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205846380..205847135hg38UCSC Ensembl
chr2:206711104..206711859hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38756
hg19756
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257882
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542484
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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