A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104617



Internal ID22013850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152451639..153075679hg38UCSC Ensembl
chrX:151620111..152244062hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38624041
hg19623952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637771
Samples
Known GenesCETN2, CSAG1, CSAG2, CSAG3, CSAG4, GABRQ, MAGEA12, MAGEA2, MAGEA2B, MAGEA3, MAGEA6, NSDHL, PNMA3, PNMA5, PNMA6A, PNMA6C, ZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104617
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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