A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884339



Internal ID22659321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95651922..95669801hg38UCSC Ensembl
chrX:94906921..94924800hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3817880
hg1917880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461426
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884339
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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