A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147165



Internal ID346347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152725536..152742753hg38UCSC Ensembl
chrX:151894208..151911466hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3817218
hg1917259
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738032
Samples
Known GenesCSAG1, CSAG4, MAGEA12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147165
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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