A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431741



Internal ID210509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101800345..101812818hg38UCSC Ensembl
chrX:101055318..101067791hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3812474
hg1912474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741741
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431741
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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