A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219722



Internal ID20786762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119814269..119815184hg38UCSC Ensembl
chr10:121573781..121574696hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38916
hg19916
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577620
Supporting Variants
Samples
Known GenesINPP5F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219722
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00022


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