A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433755



Internal ID212458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4845121..4858535hg38UCSC Ensembl
chrX:4763162..4776576hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3813415
hg1913415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv562n206
Supporting Variantsnssv17736168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433755
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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