A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438224



Internal ID22496094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97528799..97530425hg38UCSC Ensembl
chr8:98541027..98542653hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381627
hg191627
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438224
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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