A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579749



Internal ID20952820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119572379..119573055hg38UCSC Ensembl
chr10:121331891..121332567hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38677
hg19677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv900n223
Supporting Variantsnssv18223544
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579749
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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