A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429337



Internal ID208187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123387371..123387636hg38UCSC Ensembl
chrX:122521222..122521487hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737478
Samples
Known GenesGRIA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429337
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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