A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257914



Internal ID21398249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102337980..102386234hg38UCSC Ensembl
chrX:101592903..101641155hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3848255
hg1948253
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730235
Supporting Variants
SamplesHG00513
Known GenesNXF2, NXF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257914
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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