A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112329



Internal ID22021562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150214465..150340179hg38UCSC Ensembl
chrX:149382695..149508434hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38125715
hg19125740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642866
Samples
Known GenesMIR2114
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112329
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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