A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432779



Internal ID211514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46495973..46497337hg38UCSC Ensembl
chrX:46355408..46356772hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381365
hg191365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432779
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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