A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536807



Internal ID20910150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:74841340..74841506hg38UCSC Ensembl
chr3:74890491..74890657hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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