A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583913



Internal ID20956984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42601734..42604250hg38UCSC Ensembl
chr10:43097182..43099698hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg382517
hg192517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235477
Samples
Known GenesZNF33B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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