A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881289



Internal ID22656264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4578538..4578700hg38UCSC Ensembl
chrX:4496579..4496741hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881289
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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