A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590275



Internal ID20963346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86567436..86568158hg38UCSC Ensembl
chr10:88327193..88327915hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590275
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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