A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107936



Internal ID22017171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:94868433..94868797hg38UCSC Ensembl
chrX:94123432..94123796hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648341
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107936
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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