A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977475



Internal ID22752410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26872678..26899149hg38UCSC Ensembl
chr8:26730195..26756666hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3826472
hg1926472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17434110
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977475
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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