A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873288



Internal ID22648233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152554106..152558965hg38UCSC Ensembl
chrX:151722578..151727437hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384860
hg194860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873288
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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