A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111637



Internal ID22020870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:310744..1184304hg38UCSC Ensembl
chrX:227411..1264234hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38873561
hg191036824
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642482
Samples
Known GenesGTPBP6, LINC00685, PPP2R3B, SHOX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111637
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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