A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108393



Internal ID22017627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104157733..104158347hg38UCSC Ensembl
chrX:103402414..103403028hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108393
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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