A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592272



Internal ID20965343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92672410..92673115hg38UCSC Ensembl
chr10:94432167..94432872hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592272
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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