A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258685



Internal ID21400648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63178945..63200001hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3821057
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730051
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258685
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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