A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383819



Internal ID22441689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:37730121..38268607hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38538487
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975785
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383819
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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