A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559411



Internal ID332444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144724947..144724998hg38UCSC Ensembl
chrX:143806468..143806519hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559411
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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