A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577702



Internal ID20950773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67818744..67819160hg38UCSC Ensembl
chr10:69578502..69578918hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220754
Samples
Known GenesDNAJC12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577702
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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