A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258388



Internal ID21398587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154555766..154645807hg38UCSC Ensembl
chrX:153783981..153874081hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3890042
hg1990101
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730207
Supporting Variants
SamplesHG00514
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B, IKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258388
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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