A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885319



Internal ID22660303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:128912306..128912422hg38UCSC Ensembl
chrX:128046284..128046400hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885319
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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