A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869712



Internal ID22644647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:80832740..80919483hg38UCSC Ensembl
chrX:80088239..80174982hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3886744
hg1986744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461126
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869712
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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