A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977125



Internal ID22752060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11700657..11703661hg38UCSC Ensembl
chr8:11558166..11561170hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg383005
hg193005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446474
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977125
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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