A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5413960



Internal ID193250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133403078..133403880hg38UCSC Ensembl
chrX:132537106..132537908hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742403
Samples
Known GenesGPC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5413960
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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