A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871292



Internal ID22646229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154460911..154460972hg38UCSC Ensembl
chrX:153689251..153689312hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432601
Samples
Known GenesPLXNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871292
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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