A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965541



Internal ID22740476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26831703..26831703hg38UCSC Ensembl
chrX:26849820..26849820hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965541
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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