A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14372887



Internal ID22293265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39776530..39776654hg38UCSC Ensembl
chrX:39635784..39635908hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182806
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14372887
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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