A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867619



Internal ID22642554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51099784..51103377hg38UCSC Ensembl
chrX:50842630..50846223hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg383594
hg193594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469068
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867619
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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