A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874319



Internal ID22649271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154400937..154401249hg38UCSC Ensembl
chrX:153629278..153629590hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448079
Samples
Known GenesDNASE1L1, RPL10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874319
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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