A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256230



Internal ID21398932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73004382..73077743hg38UCSC Ensembl
chrX:72224221..72297582hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3873362
hg1973362
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730106
Supporting Variants
SamplesHG00731
Known GenesPABPC1L2A, PABPC1L2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256230
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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