A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257619



Internal ID21400178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135147415..135225242hg38UCSC Ensembl
chrX:134281342..134359186hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3877828
hg1977845
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730233
Supporting Variants
SamplesNA19239
Known GenesCXorf48
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257619
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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