A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416956



Internal ID196164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:99646363..99656282hg38UCSC Ensembl
chrX:98901361..98911280hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg389920
hg199920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741666
Samples
Known GenesXRCC6P5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416956
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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