A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417733



Internal ID196922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113727957..113728168hg38UCSC Ensembl
chrX:112971237..112971448hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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