A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557597



Internal ID20930668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121100305..121131677hg38UCSC Ensembl
chr9:123862583..123893955hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3831373
hg1931373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279754
Samples
Known GenesCNTRL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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