A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262630



Internal ID20471848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133661562..133661648hg38UCSC Ensembl
chrX:132795590..132795676hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764070
Supporting Variants
Samples
Known GenesGPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262630
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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