A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258296



Internal ID21398024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64486396..64498522hg38UCSC Ensembl
chr9:69498814..69510940hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3812127
hg1912127
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258296
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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