A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641596



Internal ID21833643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86834564..86835431hg38UCSC Ensembl
chrX:86089567..86090434hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105283
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641596
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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