A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105417



Internal ID22014650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133629621..133629704hg38UCSC Ensembl
chrX:132763649..132763732hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645509
Samples
Known GenesGPC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105417
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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