A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562897



Internal ID335837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103607585..103607636hg38UCSC Ensembl
chrX:102862513..102862564hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38564
hg19564
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741787
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562897
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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