A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553254



Internal ID326519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25042022..25042028hg38UCSC Ensembl
chrX:25060139..25060145hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739763
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553254
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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