A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257111



Internal ID21399628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115726314..115729676hg38UCSC Ensembl
chrX:114965460..114971814hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383363
hg196355
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730056
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257111
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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