A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257510



Internal ID21399853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76141674..76153292hg38UCSC Ensembl
chrX:75361509..75373127hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3811619
hg1911619
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730272
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257510
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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