A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446897



Internal ID22504767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47302678..47317875hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3815198
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446897
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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