A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885863



Internal ID22660849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57468756..57485087hg38UCSC Ensembl
chrX:57495189..57511520hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3816332
hg1916332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463499
Samples
Known GenesFAAH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885863
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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