A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258207



Internal ID21400839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41471461..41508333hg38UCSC Ensembl
chr9:68149091..68186040hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3836873
hg1936950
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730044
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258207
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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