A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590967



Internal ID20964038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111315102..111316018hg38UCSC Ensembl
chr10:113074860..113075776hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590967
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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