A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107116



Internal ID22016349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123941658..123951224hg38UCSC Ensembl
chrX:123075508..123085074hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg389567
hg199567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107116
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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