A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536790



Internal ID20910133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24366572..24367860hg38UCSC Ensembl
chr2:24589441..24590729hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536790
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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