A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884497



Internal ID22659480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54536086..54536171hg38UCSC Ensembl
chrX:54562519..54562604hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17462890
Samples
Known GenesGNL3L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884497
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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