A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869331



Internal ID22644266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70210408..70226816hg38UCSC Ensembl
chrX:69430258..69446666hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3816409
hg1916409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869331
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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