A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256035



Internal ID21400465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64459338..64561708hg38UCSC Ensembl
chr9:69471756..69574126hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38102371
hg19102371
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730150
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256035
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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