A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588859



Internal ID20961930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:73141998..73142625hg38UCSC Ensembl
chr10:74901756..74902383hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231887
Samples
Known GenesECD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588859
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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