A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5419806



Internal ID198929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140679173..140688914hg38UCSC Ensembl
chrX:139761338..139771079hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg389742
hg199742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv580n206
Supporting Variantsnssv17742699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5419806
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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