A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359250



Internal ID22584919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25718859..25772058hg38UCSC Ensembl
chr10:26007788..26060987hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3853200
hg1953200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5978982
Supporting Variants
Samples
Known GenesLINC00836
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359250
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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