A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221247



Internal ID20788287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119624318..119624392hg38UCSC Ensembl
chr10:121383830..121383904hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581865
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221247
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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