A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108353



Internal ID22017586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:98831108..98831165hg38UCSC Ensembl
chrX:98086106..98086163hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108353
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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