A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429187



Internal ID208039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154505414..154510415hg38UCSC Ensembl
chrX:153733745..153738746hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg385002
hg195002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738125
Samples
Known GenesFAM3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429187
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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