A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582997



Internal ID20956068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93271762..93272533hg38UCSC Ensembl
chr10:95031519..95032290hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582997
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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