A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219687



Internal ID20786727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61946740..61947433hg38UCSC Ensembl
chr10:63706499..63707192hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38694
hg19694
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576950
Supporting Variants
Samples
Known GenesARID5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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