A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562803



Internal ID335746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25286787..25286790hg38UCSC Ensembl
chrX:25304904..25304907hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562803
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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