A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886029



Internal ID22661016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129874340..129875018hg38UCSC Ensembl
chrX:129008316..129008994hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444866
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886029
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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