A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669854



Internal ID21618159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60775308..60780330hg38UCSC Ensembl
chr1:61240980..61246002hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg385023
hg195023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065688
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669854
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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