A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588096



Internal ID20961167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63062468..63062662hg38UCSC Ensembl
chr10:64822228..64822422hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220244
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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