A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112426



Internal ID22021659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101602193..101616307hg38UCSC Ensembl
chrX:100857177..100871297hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3814115
hg1914121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641645
Samples
Known GenesARMCX6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112426
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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