A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104671



Internal ID22013904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55184526..55652521hg38UCSC Ensembl
chrX:55210959..55678954hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38467996
hg19467996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640030
Samples
Known GenesFOXR2, MAGEH1, MIR4536-1, PAGE3, PAGE5, USP51
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104671
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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