A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111154



Internal ID22020387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133661581..133661652hg38UCSC Ensembl
chrX:132795609..132795680hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639003
Samples
Known GenesGPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111154
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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