A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258628



Internal ID21399971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120075637..120172547hg38UCSC Ensembl
chrX:119209602..119306402hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3896911
hg1996801
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730157
Supporting Variants
SamplesNA19238
Known GenesRHOXF1, RHOXF2, RHOXF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258628
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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