A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257104



Internal ID21397908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51692405..51703134hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3810730
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730130
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257104
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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