A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877392



Internal ID22652356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95058137..95125324hg38UCSC Ensembl
chrX:94313136..94380323hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3867188
hg1967188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17450080
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877392
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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