A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885286



Internal ID22660270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127338374..127560328hg38UCSC Ensembl
chrX:126472357..126694309hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38221955
hg19221953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438928
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885286
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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