A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257639



Internal ID21400528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43231770..43232427hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38658
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730111
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257639
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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