A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257991



Internal ID21400135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55457333..55493921hg38UCSC Ensembl
chrX:55483766..55520354hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3836589
hg1936589
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730209
Supporting Variants
SamplesNA19238
Known GenesUSP51
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257991
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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