A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550885



Internal ID20924027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33651166..33651712hg38UCSC Ensembl
chr3:33692658..33693204hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38547
hg19547
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262063
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550885
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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