A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577234



Internal ID20950305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123543433..123544090hg38UCSC Ensembl
chr10:125302949..125303606hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222994
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577234
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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