A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258153



Internal ID21399783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73004367..73079523hg38UCSC Ensembl
chrX:72224206..72299362hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3875157
hg1975157
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730106
Supporting Variants
SamplesHG00733
Known GenesPABPC1L2A, PABPC1L2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258153
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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