A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428978



Internal ID207836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141906090..141906785hg38UCSC Ensembl
chrX:140993876..140994571hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38696
hg19696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742767
Samples
Known GenesMAGEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428978
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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