A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231744



Internal ID20798784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124750991..124751222hg38UCSC Ensembl
chr10:126439560..126439791hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231744
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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