A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3546091



Internal ID22415090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6218929..6220353hg38UCSC Ensembl
chrX:6136970..6138394hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381425
hg191425
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453060, nssv14459197, nssv14459288, nssv14463227
SamplesNA19238, NA19239, NA19240, HG00733
Known GenesNLGN4X
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3546091
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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