A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555102



Internal ID328268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106467197..106467223hg38UCSC Ensembl
chrX:105710427..105710453hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381062
hg191062
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555102
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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