A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256190



Internal ID21398304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52920148..52935790hg38UCSC Ensembl
chrX:52949338..52964999hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3815643
hg1915662
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730076
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256190
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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