A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562600



Internal ID335549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154102987..154103038hg38UCSC Ensembl
chrX:153368439..153368490hg19UCSC Ensembl
CytobandXq28
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 Variantsnssv17738103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562600
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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