A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419002



Internal ID198151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48333837..48375837hg38UCSC Ensembl
chrX:48193272..48235269hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3842001
hg1941998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736844
Samples
Known GenesSSX3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419002
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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