A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14413037



Internal ID22148297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:82739299..82741946hg38UCSC Ensembl
chrX:81994748..81996954hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg382648
hg192207
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3177739
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14413037
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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