A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429038



Internal ID22170562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6218986..6219315hg38UCSC Ensembl
chrX:6137027..6137356hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3185963
Supporting Variants
SamplesHG00514
Known GenesNLGN4X
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14429038
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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