A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422560



Internal ID201602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21968051..21968103hg38UCSC Ensembl
chrX:21986169..21986221hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739610
Samples
Known GenesSMS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422560
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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