A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589452



Internal ID20962523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33953484..33953879hg38UCSC Ensembl
chr10:34242412..34242807hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589452
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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