A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14351530



Internal ID22263905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6219007..6220343hg38UCSC Ensembl
chrX:6137048..6138384hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeOTHER complex substitution
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3187983
Supporting Variants
SamplesNA19238
Known GenesNLGN4X
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14351530
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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