A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138849



Internal ID338033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24241000..24258100hg38UCSC Ensembl
chrX:24259117..24276217hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3817101
hg1917101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138849
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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