A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044306



Internal ID21953589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133709486..133709486hg38UCSC Ensembl
chrX:132843514..132843514hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg381066
hg191066
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649273
Samples
Known GenesGPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044306
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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