A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765805



Internal ID20541665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6219006..6220350hg38UCSC Ensembl
chrX:6137047..6138391hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381345
hg191345
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16275896
Samples
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765805
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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