A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419639



Internal ID198769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154785860..154785958hg38UCSC Ensembl
chrX:154014135..154014233hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738150
Samples
Known GenesMPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419639
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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