A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878232



Internal ID22653197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:87716998..87717065hg38UCSC Ensembl
chrX:86971998..86972065hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464990
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878232
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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