A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877507



Internal ID22652471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233763..47233815hg38UCSC Ensembl
chrX:47093162..47093214hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457871
Samples
Known GenesUSP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877507
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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