A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459197



Internal ID22269409
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3546091
Supporting Variants
SamplesNA19239
Known GenesNLGN4X
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14459197
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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