A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427518



Internal ID206422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6261136..6496602hg38UCSC Ensembl
chrX:6179177..6414643hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38235467
hg19235467
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739054
Samples
Known GenesMIR4770
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427518
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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