A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878904



Internal ID22653870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42727836..42729476hg38UCSC Ensembl
chrX:42587087..42588727hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381641
hg191641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461685
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878904
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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