A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881297



Internal ID22656272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115307866..115309893hg38UCSC Ensembl
chrX:114542431..114544458hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg382028
hg192028
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2294n209
Supporting Variantsnssv17437196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881297
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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