A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535900



Internal ID20909253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240474052..240476217hg38UCSC Ensembl
chr2:241413469..241415634hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382166
hg192166
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18257470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535900
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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