A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258292



Internal ID21398858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153148416..153270263hg38UCSC Ensembl
chrX:152414899..152515909hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38121848
hg19101011
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730148
Supporting Variants
SamplesHG00731
Known GenesMAGEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258292
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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