A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589278



Internal ID20962349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100322384..100323540hg38UCSC Ensembl
chr10:102082141..102083297hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224836
Samples
Known GenesPKD2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589278
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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