A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592108



Internal ID20965179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70475823..70478073hg38UCSC Ensembl
chr10:72235579..72237829hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382251
hg192251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592108
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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