A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257248



Internal ID21397883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102230490..102348649hg38UCSC Ensembl
chrX:101485484..101603572hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38118160
hg19118089
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730235
Supporting Variants
SamplesHG00512
Known GenesNXF2, NXF2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257248
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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