A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257897



Internal ID21398236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152720940..152744624hg38UCSC Ensembl
chrX:151892991..151911609hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3823685
hg1918619
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730087
Supporting Variants
SamplesHG00513
Known GenesCSAG1, CSAG4, MAGEA12
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257897
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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