A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577840



Internal ID20950911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:106568712..106569602hg38UCSC Ensembl
chr10:108328470..108329360hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577840
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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