A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880467



Internal ID22655437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115307786..115309957hg38UCSC Ensembl
chrX:114542351..114544522hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg382172
hg192172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2294n209
Supporting Variantsnssv17432056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880467
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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