A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578883



Internal ID20951954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36568145..36569234hg38UCSC Ensembl
chr10:36857073..36858162hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381090
hg191090
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578883
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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