A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434110



Internal ID22491980
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 StatusS
Merged Variantsnsv5977475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434110
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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