A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232364



Internal ID20799404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26139272..26139732hg38UCSC Ensembl
chr10:26428201..26428661hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583935
Supporting Variants
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232364
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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