A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14403218



Internal ID22323170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54534158..54535602hg38UCSC Ensembl
chrX:54560591..54562035hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg381445
hg191445
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3178102
Supporting Variants
SamplesNA19240
Known GenesGNL3L
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14403218
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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