A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187983



Internal ID22340017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6219007..6220343hg38UCSC Ensembl
chrX:6137048..6138384hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351530, nssv14351526, nssv14351527, nssv14351531, nssv14351528, nssv14351529, nssv14351532
SamplesHG00512, NA19238, NA19239, HG00732, NA19240, HG00733, HG00514
Known GenesNLGN4X
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Commentscomplex variant
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3187983
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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