A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420673



Internal ID199770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41467407..41468361hg38UCSC Ensembl
chrX:41326660..41327614hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38955
hg19955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736575
Samples
Known GenesNYX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420673
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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