A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105664



Internal ID22014897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153060573..153075060hg38UCSC Ensembl
chrX:152228933..152243443hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3814488
hg1914511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643488
Samples
Known GenesPNMA6A, PNMA6C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105664
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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