A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535859



Internal ID20909213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197567312..197567528hg38UCSC Ensembl
chr2:198432036..198432252hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257119
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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