A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372980



Internal ID22598649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:25571452..25685348hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38113897
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372980
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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