A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884484



Internal ID22659467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122630349..122630907hg38UCSC Ensembl
chrX:121764202..121764760hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884484
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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