A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887306



Internal ID22662298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:93054535..93104064hg38UCSC Ensembl
chrX:92309534..92359063hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg3849530
hg1949530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887306
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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