A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975318



Internal ID22750253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48658736..48675794hg38UCSC Ensembl
chr10:49866781..49883839hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3817059
hg1917059
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353690
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975318
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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