A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591215



Internal ID20964286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73629760..73629969hg38UCSC Ensembl
chr10:75389518..75389727hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591215
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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