A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104295



Internal ID22013528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56236832..56710098hg38UCSC Ensembl
chrX:56263265..56736531hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38473267
hg19473267
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640386
Samples
Known GenesKLF8, UBQLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104295
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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