A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5430515



Internal ID209321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68517102..68517277hg38UCSC Ensembl
chrX:67736944..67737119hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740533
Samples
Known GenesYIPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5430515
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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