A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224555



Internal ID20791595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36631333..36631993hg38UCSC Ensembl
chr10:36920261..36920921hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6589230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224555
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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