A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17444789



Internal ID22502659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77391769..77392151hg38UCSC Ensembl
chr8:78304005..78304387hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976301
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17444789
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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