A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979890



Internal ID22754825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35697173..35700463hg38UCSC Ensembl
chr1:36162774..36166064hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383291
hg193291
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17380219
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979890
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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