A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257630



Internal ID21400180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41770308..42145041hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38374734
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730078
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257630
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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