A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420888



Internal ID199979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123853819..123858226hg38UCSC Ensembl
chrX:122987669..122992076hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg384408
hg194408
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420888
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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