A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256497



Internal ID21399793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135127506..135236864hg38UCSC Ensembl
chrX:134261434..134370811hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38109359
hg19109378
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730233
Supporting Variants
SamplesHG00733
Known GenesCXorf48
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256497
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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