A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534311



Internal ID310125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15282921..15282971hg38UCSC Ensembl
chrX:15301043..15301093hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739392
Samples
Known GenesASB11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534311
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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