A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867860



Internal ID22642795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1666316..1666671hg38UCSC Ensembl
chrX:1785209..1785564hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867860
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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