A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874942



Internal ID22649896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45434811..45434871hg38UCSC Ensembl
chrX:45294056..45294116hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874942
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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