A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877168



Internal ID22652131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88735668..88744704hg38UCSC Ensembl
chrX:87990669..87999705hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg389037
hg199037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877168
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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