A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256459



Internal ID21400338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154558378..154613801hg38UCSC Ensembl
chrX:153786593..153842057hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3855424
hg1955465
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730207
Supporting Variants
SamplesNA19239
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B, IKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256459
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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