A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258796



Internal ID21399442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55480160..55521060hg38UCSC Ensembl
chrX:55506593..55547493hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3840901
hg1940901
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730209
Supporting Variants
SamplesHG00732
Known GenesUSP51
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258796
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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