A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109846



Internal ID22019079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16803119..16815169hg38UCSC Ensembl
chrX:16821242..16833292hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3812051
hg1912051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649438
Samples
Known GenesTXLNG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109846
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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