A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980284



Internal ID22755219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81551395..81551853hg38UCSC Ensembl
chr6:82261112..82261570hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38459
hg19459
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447802
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980284
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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