A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649273



Internal ID21841320
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 StatusS
Merged Variantsnsv6044306
Supporting Variants
Samples
Known GenesGPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649273
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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